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家族性丹迪-沃克畸形伴巨头畸形、面部异常、发育迟缓及脑干发育不全:兄弟病例的产前诊断及产后结局。一种新综合征?

Familial Dandy-Walker malformation associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis: prenatal diagnosis and postnatal outcome in brothers. A new syndrome?

作者信息

Chitayat D, Moore L, Del Bigio M R, MacGregor D, Ben-Zeev B, Hodgkinson K, Deck J, Stothers T, Ritchie S, Toi A

机构信息

Prenatal Diagnosis Program, Toronto Hospital, Ontario, Canada.

出版信息

Am J Med Genet. 1994 Oct 1;52(4):406-15. doi: 10.1002/ajmg.1320520404.

Abstract

Brothers are reported with an apparently new constellation of manifestations including Dandy-Walker complex (DWC), migrational brain disorder, macrocephaly, and facial anomalies. The first brother presented at birth, the second was detected prenatally with DWC and the pregnancy terminated. Fetal brain histopathology showed DWC associated with brainstem dysgenesis. Inheritance is likely autosomal or X-linked recessive. An extensive review of the differential diagnosis of DWC is provided.

摘要

据报道,兄弟俩出现了一系列明显的新症状,包括丹迪-沃克综合征(DWC)、脑移行障碍、巨头畸形和面部异常。第一个兄弟出生时就出现了这些症状,第二个在产前被检测出患有DWC,随后终止了妊娠。胎儿脑组织病理学检查显示DWC与脑干发育不全有关。遗传方式可能为常染色体或X连锁隐性遗传。本文对DWC的鉴别诊断进行了广泛综述。

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