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- W2030338392 abstract "We present a father and son with congenital foot deformity. The father at age 41 years used crutches and the son at 7 years walked unaided. Both had atrophy and weakness of lower leg muscles and mild proximal and hand intrinsic weakness. Knee and ankle myotactic reflexes were absent and sensation was intact. Creatine kinase level was normal, nerve conduction studies were normal and electromyography showed chronic neurogenic change. In both, nerve biopsies were normal and muscle biopsies showed type 1 predominance. The boy's serum hexosaminidase, spinal MRI and SMN gene were normal. This may be the first well documented example of congenital autosomal dominant distal spinal muscular atrophy affecting legs and arms." @default.
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- W2030338392 date "1998-08-01" @default.
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- W2030338392 title "Congenital autosomal dominant distal spinal muscular atrophy" @default.
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- W2030338392 doi "https://doi.org/10.1016/s0960-8966(98)00042-x" @default.
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