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丹迪-沃克畸形(变异型)、多囊性发育不良肾和肝纤维化:一种独特的病症还是梅克尔综合征?

Dandy-Walker malformation (variant), cystic dysplastic kidneys, and hepatic fibrosis: a distinct entity or Meckel syndrome?

作者信息

Walpole I R, Goldblatt J, Hockey A, Knowles S

机构信息

Clinical Genetics Unit, King Edward Memorial Hospital for Women, Subiaco, Australia.

出版信息

Am J Med Genet. 1991 Jun 1;39(3):294-8. doi: 10.1002/ajmg.1320390310.

Abstract

Dandy-Walker malformation is an unusual finding in Meckel syndrome, which characteristically presents with encephalocele, polydactyly, and cystic renal disease. We report on a family in which three nonviable brothers had Dandy-Walker malformations (variant) with associated enlarged cystic dysplastic kidneys and hepatic fibrosis. The consistent segregation of these abnormalities in all three sibs in the absence of polydactyly and encephalocele suggested the possibility of a distinct syndrome. The clinicopathological findings of the disorder are described and discussed in the context of the phenotypic spectrum of Meckel syndrome.

摘要

丹迪-沃克畸形在梅克尔综合征中是一种不常见的表现,梅克尔综合征的典型特征是脑膨出、多指畸形和多囊肾病。我们报告了一个家族,其中三个无法存活的兄弟患有丹迪-沃克畸形(变异型),伴有囊性发育不良性肾肿大和肝纤维化。在没有多指畸形和脑膨出的情况下,所有三个兄弟姐妹中这些异常的一致分离提示了一种独特综合征的可能性。本文在梅克尔综合征的表型谱背景下描述并讨论了该疾病的临床病理发现。

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