Clinico-pathological diagnosis of Facioscapulohumeral Dystrophy in a 22-year-old Male
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2.03–6.8 per 100,000 individuals. FSHD is the third most common type of muscular dystrophy after the Duchene muscular dystrophy and myotonic dystrophy. To the best of our knowledge, the current case re...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Knowledge E
2021-03-01
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Series: | Sudan Journal of Medical Sciences |
Subjects: | |
Online Access: | https://doi.org/10.18502/sjms.v16i1.8945 |