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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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更新时间:2025/2/3 11:50:24