All About SCA3/MJD

  Рет қаралды 2,075

National Ataxia Foundation

National Ataxia Foundation

Күн бұрын

Spinocerebellar Ataxia 3 or Machado-Joseph Disease is one of the most common forms of Ataxia but is still a relatively rare disease. The National Ataxia Foundation is proud to host this webinar presented by Dr. Jennifer Faber on February 13th, 2022. In "All About SCA3/MJD", she gave an overview of the causes and symptoms of the disease, the typical diagnostic journey for those affected, and what to expect for clinical care.
For more on SCA3/MJD, register for our upcoming webinar on Thursday, Feb 16 here: us02web.zoom.us/webinar/regis...
For more information on Ataxia, please visit our website: www.ataxia.org
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About the Speaker:
Dr. Jennifer Faber is working as a neurologist at the Department of Neurology, University Hospital Bonn, and clinical investigator at the Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany. She received a pre-diploma in Mathematics from Bon University, and graduated with an MD and doctor of medicine degree. After a research stay at Stanford University, she continued her research at the DZNE on MR imaging of Ataxias and disease modeling.
She uses multimodal MRI acquired at 3T as well as high-field 7T to assess structural alterations. A particular focus is the investigation of structural alterations of the cerebellum and brainstem, that might serve as imaging biomarkers in the pre-ataxic stages of spinocerebellar ataxias (SCA). Eventually, this leads to improved data-driven models of the disease course in particular in early pre-symptomatic stages, where clinical scales are lacking sensitivity. Together with Heike Jacobi she initiated the SCA Global Young Investigator Initiative, a platform for scientific exchange amongst young researchers and for education and training purposes. Dr. Faber is Fellow of the Hertie Network of Excellence in Clinical Neuroscience.
About the Series:
NAF is producing a series of monthly educational webinars that focus on one type of Ataxia at a time. Each month we will feature a different type. Clinical experts will join us to take a look at the causes and symptoms of the disease, the typical diagnostic journey for those affected, and what to expect for clinical care. Research experts will teach us how the disease is studied and give an overview of the current state of research and drug development.

Пікірлер: 6
@steveb978
@steveb978 4 ай бұрын
Hi people im 62 years old man i live in Canada from Portuguese Acores parents my grandmother and mother suffered from this ataxia it was horrible seeing them go through this from what i understand that i have a 50\50 chance of developing this gene i so far have been lucky with no symptoms but my hart goes out to all who suffer from this this is a horrible disseise that takes every thing away from those who suffer it i stared smoking cannabis at the age of 20 and still do today i have one sister who also dose cannabis and did not develop this gene So i have 2 children and they also use cannabis but we all started young using cannabis im no expert but i think it had something to do with it but i never was big on drinking alcohol and have been alcohol free for 35 years
@anai007
@anai007 3 ай бұрын
My sister and me sufer from this terible disease we are in whelchair in nursing home in Croatia😢😢
@hokwanwai1433
@hokwanwai1433 Жыл бұрын
I am 56 year old from Hong Kong Cloud you treatment method Spinocerebellar Ataxia 6 thx
@steveb978
@steveb978 4 ай бұрын
use cannabis it helps
@joshivrujesh4695
@joshivrujesh4695 Жыл бұрын
I am 37 year old from India i have 2 child i am so scared about my child please help us
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