Alpha 1 Antitrypsin Deficiency Causes Symptoms Diagnosis Treatment Pathology....!

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Channel Title : Rehealthify

Views : 14998

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Published Date : 2014-07-21T21:20:39.000Z

See much more honest health information at: http://www.rehealthify.com/ Rehealthify offers reliable, up-to-date health information, anytime, anywhere, for free. -- video script below -- Alpha-1 antitrypsin deficiency (AAT deficiency) is an inherited condition that raises your risk for lung and liver disease. Alpha-1 antitrypsin (AAT) is a protein that protects the lungs. The liver makes it. If the AAT proteins aren't the right shape, they get stuck in the liver cells and can't reach the lungs. Symptoms of AAT deficiency include • Shortness of breath and wheezing • Repeated lung infections • Tiredness • Rapid heartbeat upon standing • Vision problems • Weight loss Some people have no symptoms and do not develop complications. Blood tests and genetic tests can tell if you have it. If your lungs are affected, you may also have lung tests. Treatments include medicines, pulmonary rehab, and extra oxygen, if needed. Severe cases may need a lung transplant. Not smoking can prevent or delay lung symptoms. NIH: National Heart, Lung, and Blood Institute
    

Channel Title : Don't Question Me

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Published Date : 2017-08-30T04:29:05.000Z

Wikipedia wiki alpha_1 antitrypsin_deficiency url? Q webcache. Aatd occurs in learn about alpha 1 antitrypsin deficiency, the symptoms of this condition, how it is diagnosed and options for treatment 21 jul 2014. Alpha 1 antitrypsin deficiency wikipedia en. What is alpha 1 antitrypsin? Alpha antitrypsin a substance present normally in the blood of all people and child's ability to make inherited through genes passed on from both parents. A genetic condition is one that can be passed on from your parents through genes 11 feb 2016 alpha 1 antitrypsin (a1at) a glycoprotein which largely produced in the liver. Googleusercontent search. Alpha 1 antitrypsin deficiency genetics home reference. It is passed from parents to their children through genes. It is a serine protease inhibitor. What is emphysema? Emphysema a condition that involves damage to the walls of air alpha 1 antitrypsin deficiency common disorder caused by reduced levels liver protection. Alpha 1 antitrypsin deficiency nord (national organization for learning about alpha (aatd) national causes, symptoms, treatments what is deficiency? American thoracic society. Alpha 1 antitrypsin deficiency ( deficiency, a1ad, or aatd) is a genetic disorder that causes defective production of alpha (a1at), leading to decreased a1at activity in the blood and lungs, deposition excessive abnormal protein liver cells 21 aug 2016 (a1at) condition which body does not make enough protects lungs from 8 2017 an inherited may cause lung disease. Of that group, about half will alpha 1 antitrypsin deficiency (a1ad) is a hereditary disorder characterized by low levels of protein called (a1at) which found in the (aatd) an inherited condition causes of, or no, (aat) blood. Its main function is to 10 jul 2017 alpha 1 antitrypsin deficiency a disease passed down from your parents that can make it hard breathe. Explore symptoms and the treatment options available alpha 1 antitrypsin deficiency (aat or deficiency) is a hereditary condition that results in reduced levels of (aat) protein blood lung disease. Alpha 1 may result in for unknown reasons, only 15 per cent people with alpha antitrypsin deficiency will show signs of liver disease childhood. Laurell noted the absence of band alpha1 alpha 1 antitrypsin (a1at) deficiency is an inherited genetic condition. Alpha1 antitrypsin deficiency background, pathophysiology alpha 1 deficiencyalpha deficiencywhat is deficiency? Causes, symptoms, treatmentalpha foundation. Pediatric alpha 1 antitrypsin deficiency shire. Alpha 1 antitrypsin deficiency and lung disease foundation children's liver alpha. Alpha one antitrypsin deficiency also can cause liver damage. Alpha 1 antitrypsin deficiency medlineplus medical encyclopedia. Find out about its causes, alpha 1 antitrypsin deficiency (alpha 1) is a genetic (inherited) condition. Alpha 1 antitrypsin deficiency occurs when a baby. Alpha 1 antitrypsin deficiency canadian liver foundation. Affected individuals often develop emphysema,
    

Channel Title : Osmosis

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Published Date : 2018-11-05T22:53:41.000Z

What is alpha-1 antitrypsin deficiency (A1AT)? A1AT deficiency is a genetic disorder where somebody has low circulating A1AT, resulting in both lung and liver problems. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : childrenshospgh

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Published Date : 2014-11-11T19:08:02.000Z

At the Center for Rare Disease Therapy at Children’s Hospital of Pittsburgh of UPMC, every child diagnosed with a rare disease receives an individualized treatment plan and family-centered care. For an appointment, consultation, or patient referral with an expert for a child diagnosed with Alpha 1 Antitrypsin Deficiency, please contact: Jodie Vento, MGC, LCGC Phone: +1-412-692-RARE or 412-692-7273 Email: RareCare@chp.edu
    

Channel Title : Hùng Long Phạm

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Published Date : 2018-01-04T03:03:11.000Z

    

Channel Title : ALPHA-1 Global

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Published Date : 2017-11-22T00:57:32.000Z

What is alpha-1 antitrypsin deficiency (A1AT)? A1AT deficiency is a genetic disorder where somebody has low circulating A1AT, resulting in both lung and liver problems. www.alpha-1global.org/advocacy-microsite
    

Channel Title : Medical Info

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Published Date : 2018-04-21T09:55:53.000Z

    

Channel Title : Health Apta

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Published Date : 2018-05-15T09:27:03.000Z

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Channel Title : TheBalancingAct

Views : 5534

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Published Date : 2017-03-17T15:03:31.000Z

Imagine-- a rare disease that’s rarely diagnosed-- because it mimics so many other diseases. We’re talking about Alpha-1 Anti-TRIP-sin Deficiency – or AAT -- a hereditary condition that may cause lung disease and liver disease. Dr. Kyle Hogarth, a Pulmonologist, at the University of Chicago and an expert in pulmonary diseases, joins us to discussAlpha-1 Anti-trip-sin Deficiency. It puts you at a higher risk for developing lung diseases, such as emphysema, as well as liver disease. It’s often linked with those conditions. But it’s a genetic condition-- passed from parents to their children.Who’s at risk of getting this condition? What tests determine if you have it? And what lifestyle changes can help patients cope with this disease? We have lots of insight. Visit: http://www.thebalancingact.com Like: https://www.facebook.com/TheBalancingActFans Follow: https://twitter.com/BalancingActTV #TheBalancingAct #BalancingAct 103264
    

Channel Title : MedicTube

Views : 109

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Published Date : 2018-08-08T20:50:48.000Z

ALPHA 1 ANTITRYPSIN DEFICIENCY Symptoms, Causes & Treatments OVERVIEW Also called AAT deficiency, alpha-1 antitrypsin deficiency is a genetic disease, which means it is passed down from your parents. It can cause serious lung disease that makes it hard to breathe. It can also cause liver disease that leads to jaundice, which makes your skin look yellowish. SYMPTOMS You might not know you have the disease until you're an adult, between the ages of 20 and 40. You may feel short of breath, especially when you try to exercise. You also may start to wheeze or have a whistling sound when you breathe. You may also get many lung infections. Other warning signs include: • Feeling tired • Your heart beats fast when you stand up • Weight loss If AAT deficiency causes problems with your liver, you might have symptoms like: • Yellowish skin or eyes • Swollen belly or legs • Coughing up blood CAUSES Alpha-1 antitrypsin deficiency runs in families. If you have it, you got it from faulty genes that both your parents passed on to you. Some people get the genes but don't get any symptoms. Or they have the mild version of the disease. TREATMENTS Although there’s no cure for AAT deficiency, you can raise the amount of AAT protein in your blood, which protects you against more lung damage. Doctors call this augmentation therapy. You may have this treatment if you get emphysema. Augmentation therapy is also called "replacement therapy." You get a new supply of AAT protein that comes from the blood of healthy human donors. You get the treatment once a week. The "replacement" alpha-1 gets into your body through an IV. You can have this done at home with the help of a technician, or you can go to a doctor's office. The goal of augmentation therapy is to slow or stop the damage in your lungs. It won't reverse the disease or heal any damage you already have.
    

Channel Title : Dr. Warraich Health Channel

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Published Date : 2017-06-04T11:01:01.000Z

Please visit: http://www.diseasesandtreatment.com for more information about diseases and treatment option. Alpha-1 ,Antitrypsin ,Deficiency,
    

Channel Title : MedicTube

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Published Date : 2018-10-12T18:55:22.000Z

ALPHA-1 ANTITRYPSIN DEFICIENCY Symptoms, Causes & Treatments OVERVIEW Also called AAT deficiency, alpha-1 antitrypsin deficiency is a genetic disease, which means it's passed down from your parents. It can cause serious lung disease that makes it hard to breathe. It can also cause liver disease that leads to jaundice, which makes your skin look yellowish. There's no cure, but treatments can help you manage your liver and breathing problems. You get the disease because your liver doesn't make enough of a protein called alpha-1 antitrypsin, or AAT. You need AAT to protect your lungs from getting broken down. Without it, infections and other irritants, like tobacco smoke, break down parts of your lung even faster. If you have AAT deficiency, you might not have any breathing symptoms until you're in your 20s or 30s. But when they start, you could feel short of breath or wheeze when you breathe, just like someone who has asthma. SYMPTOMS You might not know you have the disease until you're an adult, between the ages of 20 and 40. You may feel short of breath, especially when you try to exercise. You also may start to wheeze or have a whistling sound when you breathe. You may also get a lot of lung infections. Other warning signs include: • Feeling tired. • Your heart beats fast when you stand up. • Weight loss. If AAT deficiency causes problems with your liver, you might have symptoms like: • Yellowish skin or eyes. • Swollen belly or legs. • Coughing up blood. A newborn baby might have jaundice, or a yellow coloring of the skin or eyes, very yellow urine, poor weight gain, an enlarged liver, and bleeding from the nose or umbilical stump. In rare cases, a skin disease called panniculitis causes hardening of the skin with painful lumps or patches. CAUSES Alpha-1 antitrypsin deficiency runs in families. If you have it, you got it from faulty genes that both your parents passed on to you. Some people get the genes but don't get any symptoms. Or they have the mild version of the disease. The broken genes you get from your parents cause you to have a low level of AAT protein in your blood. It can build up in the liver instead of going into your bloodstream. That buildup in your liver causes liver disease. The shortage of AAT protein in your bloodstream leads to lung disease. TREATMENTS Although there’s no cure for AAT deficiency, you can raise the amount of AAT protein in your blood, which protects you against more lung damage. Doctors call this augmentation therapy. You may have this treatment if you get emphysema. Augmentation therapy is also called "replacement therapy." You get a new supply of AAT protein that comes from the blood of healthy human donors. You get the treatment once a week. The "replacement" alpha-1 gets into your body through an IV. You can have this done at home with the help of a technician, or you can go to a doctor's office. The goal of augmentation therapy is to slow or stop the damage in your lungs. It won't reverse the disease or heal any damage you already have. You will need these treatments throughout your life. Depending on how you're doing, you also may get medication that you breathe into your lungs with an inhaler. Doctors call this a bronchodilator, meaning that it opens your airways. If your breathing trouble leads to low levels of oxygen in your blood, you might need to get extra oxygen through a mask or nosepiece. Your doctor will also give you a referral for pulmonary rehab to help you breathe better.
    

Channel Title : Osmosis

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Published Date : 2017-10-31T22:00:33.000Z

What is hemochromatosis? Hemochromatosis is a genetic disorder where the body isn’t able to regulate its iron absorption. Iron levels in the body build up over time and damage the liver as well as other organs, through the generation of free radicals. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : The Prairie Doc

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Published Date : 2018-01-19T02:46:35.000Z

Alpha-1 Antitrypsin Deficiency - Anne Hovey, Diagnosed with Alpha-1 Antitrypsin Deficiency
    

Channel Title : Julie MacNeil

Views : 879

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Published Date : 2017-05-08T21:58:39.000Z

Julie MacNeil explains how she learned about the dangers of Alpha-1 Antitrypsin Deficiency.
    

Channel Title : iMEDTracker - Medication Reminder App

Views : 389

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Published Date : 2017-09-08T03:30:42.000Z

Alpha 1 antitrypsin deficiency is a debilitating disease that leads to severe lung problems such as COPD and liver failure called cirrhosis. This disease leads to early death!! Alpha 1 antitrypsin protects against breakdown of protein in the lungs and liver but when it is not there it could lead to severe architectural damage. Pulmonary function tests are done to evaluate for lung problems and they normally show Finding similar to the obstructive lung disease called chronic obstructive lung disease or COPD also called emphysema. Now physicians may get suspicious and test for alpha-1 antitrypsin deficiency especially if you develop COPD early in life such as thirties and forties or develop liver problems without any other cause. And especially also if you have COPD but you never smoked. alpha 1 antitrypsin deficiency, what is alpha 1 antitrypsin deficiency, what is alpha 1 antitrypsin, treatment of alpha 1 antitrypsin deficiency,
    

Channel Title : Osmosis

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Published Date : 2016-01-15T19:43:29.000Z

What is Wilson's disease (Wilson disease)? You usually take in more copper than your body needs every day, and any excess is excreted. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : MariVi Deliz

Views : 4519

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Published Date : 2016-02-09T19:31:10.000Z

A heartfelt short documentary profiling three families affected by the genetic condition, Alpha-1 Antitrypsin Deficiency. Three generations of the Quill family have been affected by Alpha-1. Jim is on the verge of a lung transplant that his wife, Marge does not want him to have. As his son, Donovan, an Alpha-1 Carrier married to Holly, also an Alpha-1 carrier are waiting for test results for their first child. Will their children also be affected by this genetic condition? Sarah and Richard Johnson's newborn son is born jaundiced. They don't know why until a pediatric hepatologist confirms their fears, Lucas has Alpha-1. His older sister is also diagnosed, but they don't take the news sitting down. John Walsh and his twin brother, Fred, both start to have breathing problems in their early 40s. When they are finally diagnosed, they realize that this must be what caused their mother's illness and death at the age of 46. When the National Institutes of Health suspends research to find a cure for Alpha-1, John is determined to see it continued. In 1995, he and two others establish the Alpha-1 Foundation. What is Alpha-1? Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic condition that can result in serious lung disease in adults and/or liver disease at any age. Learn more: http://.alpha1.org/what-is-alpha-1 Director/Producer/Camera/Sound: Maria Virginia Deliz Alpha-1 Foundation
    

Channel Title : Rajeev Ranjan Gupta

Views : 1376

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Published Date : 2017-02-24T12:25:48.000Z

    

Channel Title : Ultimate Health and Home Remedies

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Published Date : 2018-06-13T00:13:02.000Z

Alpha-1 antitrypsin deficiency (AAT deficiency) is an inherited condition that raises your risk for lung and liver disease. Alpha-1 antitrypsin (AAT) is a protein that protects the lungs. For more videos Subscribe Us: https://goo.gl/Xj2GQZ Don't Forget to LIKE, SHARE & COMMENT Thank You So Much By : Ultimate Health and Home Remedies Check out new videos of Ultimate Health and Home Remedies Here : https://goo.gl/mGbSAB
    

Channel Title : Osmosis

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Published Date : 2018-10-30T17:33:16.000Z

What are inclusion body myopathies? Inclusion body myopathies are a group of muscle diseases characterized by the presence of abnormal protein inclusions within muscle fibers. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : yayamensun

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Published Date : 2016-03-04T21:55:25.000Z

Alpha-1 Education Day in Cleveland, OH September 19, 2015 Speaker: Kim Brown, Certified Genetic Counselor, Alpha-1 Foundation Genetic Counseling Program
    

Channel Title : Joshua Brown

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Published Date : 2016-06-10T06:00:06.000Z

    

Channel Title : iLearn VN

Views : 239

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Published Date : 2018-07-07T14:47:45.000Z

Thiếu Alpha-1 antitrypsin (A1AT) là gì? Thiếu A1AT là một bệnh do rối loạn di truyền, khi sự hiện diện A1AT trong cơ thể thấp dẫn đến các vấn đề ở phổi và gan. ------------------------------------------------------------------ ▪️ Đăng ký kênh: https://bit.ly/2v32PZN ▪️ Xem thêm những nội dung liên quan: https://bit.ly/2IFiGUP Chúng tôi thu thập, tổ chức và xây dựng các chương trình đào tạo trực tuyến đại chúng mở nhằm thích ứng với các xu thế việc làm trong tương lai. ▪️ Website: http://ilearnvn.org Hãy liên kết với chúng tôi qua các trang mạng xã hội: ▪️ Fanpage: https://facebook.com/ilearnvn.org ▪️ FB Group: https://www.facebook.com/groups/1876886062384222/ Hãy cho chúng tôi biết ý kiến của bạn về video. Chúng tôi sẵn lòng trả lời câu hỏi của bạn. @iLearnVN @OsmoseIt Bản quyền: - Video: Osmosis - Alpha-1 Antitrypsin Deficiency - causes, symptoms, diagnosis, treatment, pathology - Licensed under a Standard Youtube License. - Music: "Piano Sonata No. 8 in A minor, K310 - Mozart" by Randolph Hokanson (ibiblio.org) - Licensed under Creative Commons License: CC BY-SA 2.0. Tất cả các video của chúng tôi có sẵn theo giấy phép Standard Youtube License. ------ Cảm ơn các thành viên trong iLearnVN Team đã hỗ trợ. Tags: #thiếuAlpha1Antitrypsin, #A1AT, #Elastase, #Protease, #khíphếthũng, #viêmphếquảnmãntính, #bệnhphổitắcnghẽnmãntính, #SERPINA1, #xơgan
    

Channel Title : Alpha-1 Foundation

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Published Date : 2016-09-12T20:19:09.000Z

25th Annual Alpha-1 National Education Conference - Miami. FL Friday, June 24th, 2016 Speaker: Mark Brantly, MD, Professor of Medicine, Molecular Genetics and Microbiology, Division of Pulmonary, Critical Care & Sleep Medicine, University of Florida College of Medicine
    

Channel Title : Alpha-1 Foundation

Views : 1523

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Published Date : 2016-09-12T19:58:14.000Z

25th Annual Alpha-1 National Education Conference - Miami. FL Friday, June 24th, 2016 Speaker: Virginia Clark, MD, Associate Program Director, Transplant Hepatology Fellowship, Assistant Professor of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, University of Florida
    

Channel Title : Osmosis

Views : 7414

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Published Date : 2018-11-07T20:56:02.000Z

What is Klüver-Bucy syndrome? Klüver-Bucy syndrome is a neurological condition caused by bilateral lesions in the temporal lobe and symptoms include hyperphagia, hyperorality, hypersexuality, docility, visual agnosia, and impaired memory. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : Katelyn Fiebke

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Published Date : 2017-05-17T17:29:09.000Z

    

Channel Title : yayamensun

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Published Date : 2015-01-20T16:47:12.000Z

Dr Sandhaus
    

Channel Title : ARS LearningCenter

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Published Date : 2016-04-18T03:22:43.000Z

DISCLAIMER: This video is for informational purposes only. The information and content in this video is not a substitute for professional medical advise, diagnosis, or treatment. For any questions, concerns, or inquiries see your primary health care physician or a licensed health care provider. Never delay or hesitate to speak with a physician because of data provided in informational documents and videos. This video will cover the following: 1)What is the Alpha-1 Antitrypsin (AAT) Deficiency 2) What are the causes of Alpha-1 AAT Deficiency 3) What are the symptoms of Alpha-1 AAT Deficiency 4) What are the possible treatments of Alpha-1 AAT Deficiency 5) What are the possible complication of AAT Alpha-1 Deficiency Credit Microsoft Word Microsoft Powerpoint Movie http://freesound.org User: Omega Grove Sound: AmberX_WPack w2.aif https://pixabay.com/en/wallpaper-colors-star-background-755962/ OSCAR If you have any comments, questions, or concerns regarding the content of this video please email arslearningcenter@gmail.com
    

Channel Title : ALPHA-1 Global

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Published Date : 2017-04-26T15:39:12.000Z

Sandra Nestler-Parr (UK) Alpha-1 Global 6th Global Patient Congress 07-08 April, 2017 Lisbon, Portugal InterContinental Hotel
    

Channel Title : 1000 Faces Scotland

Views : 1714

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Published Date : 2016-12-20T16:57:35.000Z

Lindsay Watsons struggle to get on the transplant list. She desperately needs new lungs. She could die anytime.
    

Channel Title : CSL Behring US

Views : 4835

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Published Date : 2015-10-22T14:43:02.000Z

Outdoor enthusiast Alice Wilson was diagnosed with Alpha-1 Antitrypsin Deficiency (Alpha-1) when she was 36 years old. Learn how a simple blood test changed her life. To learn more about CSL Behring delivering on its promise to people with life-threatening medical conditions, visit http://www.cslbehring.com/patient-commitment/personal-stories.htm. Follow us on Social Media: http://www.twitter.com/CSLBehring https://www.linkedin.com/company/csl-behring
    

Channel Title : Osmosis

Views : 32568

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DisLikes : 11

Published Date : 2017-10-16T23:29:21.000Z

What is 5-alpha reductase deficiency? 5-alpha reductase deficiency is a genetic condition affecting male sexual development before birth and during pregnancy. Find more videos at http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.
    

Channel Title : ALPHA-1 Global

Views : 583

Likes : 4

DisLikes : 0

Published Date : 2017-04-26T15:37:11.000Z

"Research Conference Summary" - Adam Wanner (USA) "Evidence for Efficacy of Intravenous Augmentation Therapy - Alan Altraja" (Estonia) "Alpha-1 Antitrypsin: Beyond Emphysema" - Sabina Jaciauskiene (Germany) "Inhaled Therapy" - Mark Brantly (USA) 6th Global Patient Congress 07-08 April, 2017 Lisbon, Portugal InterContinental Hotel http://www.alpha-1global.org
    

Channel Title : ALPHA-1 Global

Views : 242

Likes : 4

DisLikes : 0

Published Date : 2017-04-26T15:36:25.000Z

"Sleep Apnea and Insomnia" - Leonardo Fuks (Israel) 6th Global Patient Congress 07-08 April, 2017 Lisbon, Portugal InterContinental Hotel http://www.alpha-1global.org
    

Channel Title : Aoife Hallahan

Views : 32

Likes : 0

DisLikes : 0

Published Date : 2017-11-29T13:50:22.000Z

    

Channel Title : GeneAidyx, LLC

Views : 1013

Likes : 11

DisLikes : 0

Published Date : 2015-04-17T19:17:08.000Z

    

Channel Title : CanadaQBank

Views : 31261

Likes : 277

DisLikes : 8

Published Date : 2013-04-08T00:28:08.000Z

Alpha-1 Antitrypsin Deficiency Instructional Tutorial Video CanadaQBank.com
    

Channel Title : MRCP Part 1 Preparation Tips, Questions & Lectures

Views : 135

Likes : 3

DisLikes : 0

Published Date : 2018-05-29T00:32:44.000Z

Subscribe to this channel: https://www.youtube.com/channel/UCKDwY2bhQtcMUZ3UFdN3Mng?sub_confirmation=1 Other Hepatology Lectures: https://www.youtube.com/playlist?list=PLfBFwAwues0mECQ6y63vV-2OZIVSfbt2K Alpha-1 antitrypsin deficiency (A1AD or AATD) is a genetic disorder that may result in lung disease or liver disease. Onset of lung problems is typically between 20 and 50 years old. This may result in shortness of breath, wheezing, or an increased risk of lung infections. Complications may include COPD, cirrhosis, neonatal jaundice, or panniculitis. A1AD is due to a mutation in the SERPINA1 gene that results in not enough alpha-1 antitrypsin (A1AT). Risk factors for lung disease include cigarette smoking and environmental dust. The underlying mechanism involves unblocked neutrophil elastase and build up of abnormal A1AT in the liver. It is autosomal co-dominant, meaning that one defective allele tends to result in milder disease than two defective alleles. The diagnosis is suspected based on symptoms and confirmed by blood tests or genetic tests. Treatment of lung disease may include bronchodilators, inhaled steroids, and when infections occur antibiotics. Intravenous infusions of the A1AT protein or in severe disease lung transplantation may also be recommended. In those with severe liver disease liver transplantation may be an option. Avoiding smoking is recommended. Vaccination for influenza, pneumococcus, and hepatitis is also recommended. Life expectancy among those who smoke is 50 years old while among those who do not smoke it is almost normal. Symptoms of alpha-1 antitrypsin deficiency include shortness of breath, wheezing, rhonchi, and rales. The patient's symptoms may resemble recurrent respiratory infections or asthma that does not respond to treatment. Individuals with A1AD may develop emphysema during their thirties or forties even without a history of significant smoking, though smoking greatly increases the risk for emphysema. A1AD causes impaired liver function in some patients and may lead to cirrhosis and liver failure (15%). In newborns, alpha-1 antitrypsin deficiency has indicators that include early onset jaundice followed by prolonged jaundice. It is a leading indication for liver transplantation in newborns. A1AT deficiency remains undiagnosed in many patients. Patients are usually labeled as having COPD without an underlying cause. It is estimated that about 1% of all COPD patients actually have an A1AT deficiency. Thus, testing should be performed for all patients with COPD, asthma with irreversible airflow obstruction, unexplained liver disease, or necrotizing panniculitis.[citation needed] The initial test performed is serum A1AT level. A low level of A1AT confirms the diagnosis and further assessment with A1AT protein phenotyping and A1AT genotyping should be carried out subsequently. The Alpha-1 Foundation offers free, confidential testing. Treatment of lung disease may include bronchodilators, inhaled steroids, and when infections occur antibiotics. Intravenous infusions of the A1AT protein or in severe disease lung transplantation may also be recommended. In those with severe liver disease liver transplantation may be an option. Avoiding smoking and getting vaccinated for influenza, pneumococcus, and hepatitis is also recommended. People with lung disease due to A1AD may receive intravenous infusions of alpha-1 antitrypsin, derived from donated human plasma. This augmentation therapy is thought to arrest the course of the disease and halt any further damage to the lungs. Long-term studies of the effectiveness of A1AT replacement therapy are not available. It is currently recommended that patients begin augmentation therapy only after the onset of emphysema symptoms. As of 2015 there are four IV augmentation therapy manufacturers in the United States, Canada, and several European countries. Intravenous (IV) therapies are the standard mode of augmentation therapy delivery. Researchers are exploring inhaled therapies. IV augmentation therapies are manufactured by the following companies and have been shown to be clinically identical to one another in terms of dosage and efficacy. Augmentation therapy is not appropriate for people with liver disease; treatment of A1AD-related liver damage focuses on alleviating the symptoms of the disease. In severe cases, liver transplantation may be necessary. more: https://en.wikipedia.org/wiki/Alpha_1-antitrypsin_deficiency
    

Channel Title : Alpha-1 Foundation Ireland

Views : 4246

Likes : 31

DisLikes : 2

Published Date : 2016-10-26T17:13:52.000Z

Commissioned by the Alpha One Foundation in collaboration with COPD Support Ireland and funded by the Health Research Board, this educational film describes the genetic condition alpha-1 antitrypsin deficiency (Alpha-1 for short). People born with Alpha-1 do not produce enough alpha-1 antitrypsin, an important protein which protects the lungs. They therefore have increased risk for the lung disease chronic obstructive pulmonary disease (COPD). 1 in 25 Irish people carry the defective gene that causes Alpha-1. For more information see www.alpha1.ie.
    

Channel Title : MD Magazine

Views : 293

Likes : 2

DisLikes : 0

Published Date : 2017-10-30T00:35:12.000Z

Alpha-1 Antitrypsin Deficiency often goes undiagnosed, or is diagnosed long after it's developed. Late diagnosis leads to worse outcomes in most conditions, but AATP is rare, so no previous studies were able to find a suitable patient population.
    

Channel Title : Don't Question Me

Views : 99

Likes : 0

DisLikes : 0

Published Date : 2017-08-30T02:06:58.000Z

Memorial sloan kettering is pancreatic cancer hereditary? Johns hopkins pathology. This study suggests that either genetic factors or shared environmental influence the risk of liver cancer. Renal pelvis, pancreatic, small intestine, liver and biliary tract, stomach, brain, breast cancers 2 jun 2015 some people have inherited gene faults that increase their risk of developing particular types cancer. But there are some factors that might increase your risk of 7 mar 2016 liver disease and inherited people with hepatitis b or c have a significantly higher developing cancer, compared to information about cancer syndromes, including risks, testing, payment legal protection 29 feb 2008 family genes linked the development been when they removed iqgap2 gene using sophisticated genetic it is likely many play role in. Liver cancer symptoms and causes mayo clinic. The iron settles in tissues throughout the body, including liver there is a slight hereditary component to cancer, but it's not very strong. Inherited genes and cancer types faqs about hepatocellular. Liver cancer screening and prevention. Ask an expert can liver cancer run in the family? Related forms genetic diseases list types, symptoms, & more webmd. Johns hopkins department of family history causes and risk factors macmillan cancer support. The liver is a does this disease have genetic or hereditary link? However, one of call us free 0808 808 00 monday to friday, 9am 8pm. Family of liver cancer genes discovered sciencedaily. Cirrhosis of the liver, how can i survive if part my liver is removed? . It's an interesting question, though, because while your family's genes play only a 4 dec 2016 what is the prognosis for people with inherited liver diseases? Of diabetes and heart disease may also develop cancer, cirrhosis, 24 mar certain diseases. Hereditary liver diseases caused by genetics boots webmdliver cancer causes, diagnosis and treatmentcancer support community. This increased risk was observed even in the subset of people without viral hepatitis. Liver diseases that can increase the risk of liver cancer include hemochromatosis and wilson's disease two most common inherited are haemochromatosis if has caused cirrhosis, becomes higher disorders cause chronic inflammation, fibrosis, cirrhosis lead to development. Because of the rarity and diversity doctor reviewed information on two most common inherited liver disease hemochromatosis alpha 1 anti trypsin deficiency their symptoms, diagnosis cancer is quite rare in uk, but increasing. Liver cancer screening and prevention liver risk factors american society. What is talcum powder? Talc resources our commitment powder safety what causes liver cancer cancerquest. Liver cancer prevention & risk factors. Hereditary hemochromatosis is a disease in which the body absorbs and stores too much iron 28 apr 2016 inherited metabolic diseases. It increases the risk of liver cancer because it causes body to pancreas is a genetic disease which means that c
    

Channel Title : the study spot

Views : 8343

Likes : 27

DisLikes : 3

Published Date : 2014-08-12T20:51:26.000Z

This video reviews the various liver metabolic disorders, such as Hereditary Hemachromatosis, Wilson's Disease, and Alpha-1 Anti-Trypsin for the USMLE Step 1. HEREDITARY HEMOCHROMATOSIS Secondary can be casued by patient constantly getting trasnfusion, parenteral, and blood disorders In primary hereditary hemochromatosis you have a defect on the HFE Gene on chromsome 6. You can have a mutation C282Y or H63D. Either one of these mutation can lead to primary hereditary hemochromatosis. Also associated with HLA-A3. HFE gene regulates a protein which regulates iron absorption form the gut. There is increased iron absorption that can't be accomodated. Treatment is constant phlebotomy or iron chleators such as deforoxamine or defurosirox. Iron toxicity will lead to increased free radicals and this can increase collagen formation and these is the pathology underying hereditary hemachromatosis. You can get micronodular cirrhosis and diabetes mellitus. You may also get bronzing of the skin as the Iron incorporates into melanin and leads to pigmentation. You may also get arrythmia and Heart failure. Joint pain (arthritis) due to pseudogout. There is also chance of bein infertile and hypogonadism Labs - you will have high iron level, high ferritin level and decreased TIBC. WILSON'S Disease This is an accumulaiton of Copper. The body normally deals with copper by absorbing from gut and in liver binds with ceruloplasmin which is then excreted into plasma and then goes into tissue. Then broken down into proteins and sent through the bile and excreted. Gene defect on 13 leads to Wilson's Disease. Pathogenesis is that it can't incorporate copper into ceruloplasmin. Decrease biliary excretion of copper. This will cause copper to back up and then there is an increased in serum levels of copper. It may accumulate to in liver to cause cirrhosis, cornea to cause keyser fleischer rings. It may lead to psychosis by accumulating in the brain. It may also leads to parkinson's type tremor WILSON'S DISEASE LAB Low ceruloplasmin, high hepatic concentration. Low copper excretion Treated with D-Penicillamine. ALPHA 1 ANTI-TRYPSIN Alpha-1 Anti-trypsin is an important protein because it can deactivate protease, elastase, cathepsin and proteinase. This is important because all of these proteins are involved in breaking things down. Defect is in protein migration. When it goes from ER to Golgi Apparatus and this can lead to accumulation of anti-trypsin in the cell and it can't be used. CLINICAL EFFECTS of Alpha-1 Anti-Trypsin. Primary problems is that you will have emphysema and bronchiectasis. Eventually lead to liver damage. Cutaneous folliculitis. It may also lead to arterial aneurysms and also associated with Wegener's Granulomatosis.
    

Channel Title : Dr.Mungli

Views : 284

Likes : 2

DisLikes : 1

Published Date : 2016-05-10T02:02:20.000Z

In this video I'm explaining answer to one of the Kaplan question posted in Kaplan medicals.

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