Meckel-Gruber syndrome

名词 n.

英文释义

名词 n.
  1. A rare, lethal ciliopathic genetic disorder characterized by renal cystic dysplasia, central nervous system malformations (occipital encephalocele), polydactyly (postaxial), hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios. uncountable

词源

Named after Johann Meckel and Georg Gruber.
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