| 单词 | Werdnig-Hoffman disease |
| 释义 | Werdnig-Hoffman disease (extremely rare) n WORD FAMILY Werdnig-Hoffman disease n 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 Hyper autosomal recessive defect, autosomal recessive disease a disease caused by the presence of two recessive mutant genes on an autosome |
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