Late‐onset facioscapulohumeral muscular dystrophy type 1 in previously undiagnosed families: Presenting clinical features in an often‐misdiagnosed disorder

Introduction/AimsIn our experience, patients with late‐onset facioscapulohumeral muscular dystrophy type 1 (FSHD1) are frequently misdiagnosed, some for many years. The aim of this report is to document this clinical experience including the presenting symptoms and misdiagnoses and to discuss the ch...

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Veröffentlicht in:	Muscle & nerve 2023-11, Vol.68 (5), p.758-762
Hauptverfasser:	Felice, Kevin J., Whitaker, Charles H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Deoxyribonucleic acid Diagnosis Differential diagnosis DNA Dystrophy Genetics Muscular dystrophy Myopathy Myositis Neuromuscular diseases Patients Polymyositis Signs and symptoms
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