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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Muscular Dystrophy, Facioscapulohumeral | Legal notice |
Other terms
Dystrophies, Facioscapulohumeral Muscular,Dystrophy, Facioscapulohumeral Muscular,Facioscapulohumeral Muscular Dystrophies,Muscular Dystrophies, Facioscapulohumeral,Progressive Muscular Dystrophy, Facioscapulohumeral Type,Facioscapulohumeral Atrophy,Atrophies, Facioscapulohumeral,Atrophy, Facioscapulohumeral,Facioscapulohumeral Atrophies,Facioscapulohumeral Type Progressive Muscular Dystrophy,Facioscapulohumeral Muscular Dystrophy,Landouzy-Dejerine Dystrophy,Dystrophies, Landouzy-Dejerine,Dystrophy, Landouzy-Dejerine,Landouzy Dejerine Dystrophy,Landouzy-Dejerine Dystrophies
Description
Muscular Dystrophy, Facioscapulohumeral: An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)
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Legal notice
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