Phenotypes for disease #02845 (CMT4H (Charcot-Marie-Tooth disease, type 4H (CMT-4H)), OMIM:609311)

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0000296669 54-y women with progressive weakness and wasting of both upper and lower limbs, trophic changes, stocking and glove hypesthesia, deep sensory loss and pes cavus. Nerve conduction velocity study showed demyelinating neuropathy. Autosomal recessive Hereditary sensorimotor neuropathy CMT4H Familial, autosomal recessive 54y - 35y - - Sherifa Ahmed Hamed 00404077
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