Can the number of deletions on gene 4q be used as an indicator for prognosis for facioscapulohumeral muscular dystrophy ?

Facioscapulohumeral muscular dystrophy (FSHD) typically presents with slowly progressive weakness of the facial muscles, scapular winging and foot drop. The severity is highly variable within and between families. The diagnosis […]

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Duchenne and Becker muscular dystrophies have similar signs and symptoms. Is there a genetic difference to inform a diagnosis?

Duchenne and Becker muscular dystrophy are part of a spectrum of disease now more correctly called dystrophinopathies, as they are due to genetic faults (mutations) in a gene called dystrophin. […]

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