Niemann-Pick disease Types A and B - causes, symptoms, diagnosis, treatment, pathology
What are Niemann-Pick disese types A and B? Niemann-Pick disease types A and B, or NPD-A and NPD-B, which are subtypes of acid sphingomyelinase or ASM deficiency, are rare, genetically inherited conditions characterized by the inability to break down a fat called sphingomyelin due to a deficiency of the enzyme, acid sphingomyelinase.
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.
Видео Niemann-Pick disease Types A and B - causes, symptoms, diagnosis, treatment, pathology канала Osmosis
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.
Видео Niemann-Pick disease Types A and B - causes, symptoms, diagnosis, treatment, pathology канала Osmosis
Показать
Комментарии отсутствуют
Информация о видео
Другие видео канала
![Niemann-Pick disease Type C - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/Fx28WYe-OW8/default.jpg)
![Cell Biology | Lysosomes: Tay-Sachs, Fabry, Gaucher, Niemann-Pick Disease](https://i.ytimg.com/vi/yXLBuy38jQM/default.jpg)
![Learn Niemann-Pick Disease Faster with Picmonic (USMLE, Step 1, Step 2 CK)](https://i.ytimg.com/vi/_jaJpWBhvnY/default.jpg)
![Frontotemporal Dementia - Howard Rosen, MD](https://i.ytimg.com/vi/vjGdUzJif5w/default.jpg)
![Duchenne & Becker muscular dystrophy - causes, symptoms, treatment & pathology](https://i.ytimg.com/vi/DGOmN6rnsNk/default.jpg)
![Frontotemporal Dementia](https://i.ytimg.com/vi/EHSdNjhkvE8/default.jpg)
![Gaucher disease - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/dd9WGb9xKEo/default.jpg)
![Friedreich’s ataxia - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/bxuMTnQTprA/default.jpg)
![Alzheimer Disease | Osmosis](https://i.ytimg.com/vi/nPT1nD6Wh6E/default.jpg)
![Treating Niemann-Pick Disease Type C](https://i.ytimg.com/vi/dpTtP6fsgew/default.jpg)
![Tay-Sachs disease - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/2z3nSnBe8Vg/default.jpg)
![Mucopolysaccharide Storage Disease Type I: Hurler, Hurler-Scheie, and Scheie syndromes](https://i.ytimg.com/vi/en9M2P8SVRE/default.jpg)
![Alpha-1 Antitrypsin Deficiency - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/pXR0RpMMrfk/default.jpg)
![Glycogen Storage Diseases](https://i.ytimg.com/vi/LuVcPNF5Slg/default.jpg)
![Digeorge syndrome (22q11.2 deletion syndrome) - causes, symptoms, & pathology](https://i.ytimg.com/vi/YdDs92gaWl8/default.jpg)
![Understanding Genetics in Niemann-Pick Disease](https://i.ytimg.com/vi/oOfE5V6BIKA/default.jpg)
![Fabry disease - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/AUkqYvZ9tn0/default.jpg)
![Prader-willi syndrome - causes, symptoms, diagnosis, treatment, pathology](https://i.ytimg.com/vi/nYvm4Rsh7t8/default.jpg)
![Fabry's Disease: What You Should Know | Anjay Rastogi, MD, PhD | UCLAMDChat](https://i.ytimg.com/vi/yZwxAODrq-g/default.jpg)
![Down syndrome (trisomy 21) - causes, symptoms, diagnosis, & pathology](https://i.ytimg.com/vi/ze_6VWwLtOE/default.jpg)