Article

The China facioscapulohumeral muscular dystrophy type 1 (FSHD1) registry: rationale for and description of a nationwide, observational cohort study

2022-09-20

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a rare, hereditary, and progressive muscular dystrophy characterized by weakness and wasting of the facial (facio-) and shoulder-upper arm (scapulo-humeral-) muscles. The clinical severity varies from nonpenetrant/asymptomatic to disability with independent ambulation loss or even wheelchair dependence. Ex...

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Literature Corpus work: 8e89ead5-af38-5f31-b924-90598173cd7f
DOI: 10.21203/rs.3.rs-2006739/v1

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