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Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant manner. It is caused by an expansion of cytosine, adenine, guanine (CAG) repeats within the huntingtin (HTT) gene, which is located on chromosome 4. This pathological expansion of CAG repeats results in the production of a mutant huntingtin protein with an abnormally long polyglutamine […]

Said Beydoun, Rare Disease Day 2022: Understanding myasthenia gravis and the impact on patients’ quality of life

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Published Online: Feb 24th 2022

Prof. Said Beydoun (Keck Medical Center of USC, University of Southern California, CA, USA), Editor-in-Chief of touchREVIEWS in Neurology, joins us for Rare Disease Day to share his perspectives and experiences in treating people with myasthenia gravis. In this interview, he discusses the impact myasthenia gravis has on quality of life, the key symptoms and the prognosis for patients.

Touch Medical Media is supporting Rare Disease Day (28 February 2022) to shine a light on healthcare inequalities for people living with rare diseases, focusing on patient quality of life and the difficulty of diagnosing patients early.

Questions:

  1. Could you give us a brief overview of myasthenia gravis and the key symptoms? (0:21)
  2. What is the impact of myasthenia gravis on quality of life? (3:17)
  3. How is myasthenia gravis managed and treated? (6:10)

Disclosures: Said Beydoun has received research grants from AB Science, Amylyx, Healey ALS Center-MGH, Ra Pharma, Sanofi and UCB. He has also been a consultant/speaker for Alexion, Alnylam, Argenx, CSL, Grifols, Mitsubishi Tanabe and Takeda.

Support: The production of this video was supported by Touch Medical Media.

Other content available in support of Rare Disease Day includes:

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