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Engelsk navneord: Werdnig-Hoffman disease

1. Werdnig-Hoffman disease (om tilstand) autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; death usually occurs in early childhood


Mindre specifikke termerautosomal recessive defect, autosomal recessive disease









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