bn:03840398n
Noun Concept
EL
meckel-gruber σύνδρομο  σύνδρομο meckel
EN
Meckel-Gruber syndrome is a rare, lethal ciliopathic genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations, polydactyly, hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios. Wikipedia
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