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Which condition are you most interested in? All conditionsBecker muscular dystrophyBethlem myopathyCentral core diseaseCharcot-Marie-Tooth disease (CMT)Congenital muscular dystrophy (CMD)Congenital myasthenic syndromeCongenital myopathyCongenital myotonic dystrophyDermatomyositisDuchenne muscular dystrophyEmery-Dreifuss muscular dystrophyFacioscapulohumeral muscular dystrophy (FSH)Fibre-type disproportionFibrodysplasia ossificans progressivaHereditary inclusion body myositisHereditary motor and sensory neuropathy (CMT)Inclusion body myositisInflammatory and autoimmune neuropathiesJuvenile dermatomysotisLambert-Eaton myasthenic syndromeLimb girdle muscular dystrophyManifesting carrier of Duchenne muscular dystrophyMcArdle�s diseaseMerosin-deficient muscular dystrophyMitochondrial myopathyMulti-minicore diseaseMyasthenia gravisMyofibrillar myopathyMyositis ossificans progressivaMyotonic disordersMyotonic dystrophy type 1Myotonic dystrophy type 2Myotubular (centronuclear) myopathyOculopharyngeal muscular dystrophyPeriodic paralysis (muscle channelopathy)PolymyositisPompe�s diseaseSpinal muscular atrophyUllrich congenital muscular dystrophyUndiagnosed
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