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Differential Diagnosis For Hyporeflexia/DTRs decreased: Hereditary, Familial, Genetic Disorders


List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Periodic paralysis, hypokalemic
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Erb's Muscular Dystrophy/Limb Girdle MD
Muscular dystrophy
Muscular dystrophy, progressive
Neuropathy, hypertrophic interstitial
Neuropathy, sensory radicular, heredit.
Peroneal muscular atrophy(Charcot Mar.)
Xeroderma pigmentosum
Mitochondrial myopathy/MERRF
Dysautonomia, familial
Facioscapulohumeral muscular dystrophy
Friedreich's Ataxia
Myotonia atrophica (Steinert's disease)
Myotonia congenita (Thomsens d.)
Nemaline myopathy
Oculocerebrorenal dystrophy/Lowe syndrome
Oculopharyngeal muscular dystrophy
Roussy-Levy syndrome
Tomaculus hereditary neuropathy
Andermann Syndrome
Giant axonal neuropathy, hereditary
Myopathy, Desmin Storage type/Sarcoplasmin bodies
Myopathy, Myotubular/Centronuclear
Ullrich Muscular Dystrophy