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一名具有水致死综合征典型特征的新生儿的致死性演变——罗马尼亚患者

Lethal evolution of a newborn with consistent features of hydrolethalus syndrome--Romanian patient.

作者信息

Belengeanu V, Viskari H, Tallila J, Lahtela J, Farcas S, Andreescu N, Stoian M, Bohiltea C L, Fryns J P

机构信息

Department of Medical Genetics, University of Medicine and Pharmacy "Victor Babes", Timisoara, Romania.

出版信息

Genet Couns. 2011;22(3):293-304.

Abstract

Hydrolethalus syndrome is a severe lethal disorder most commonly found in Finland. We present a lethal case of complex congenital malformation in a Romanian family who showed multiple signs described in hydrolethalus syndrome. Our case presented the specific characteristics: macrocephaly, midline cleft-lip, cleft palate, polydactyly of both hands and feet but without occipitoschisis, considered as the pathognomonic sign of the syndrome. Sequencing analysis of HYLS1 did not identify the point mutation present in the Finnish cases or other mutations in this gene.

摘要

水致死综合征是一种严重的致死性疾病,最常见于芬兰。我们报告了罗马尼亚一个家族中一例复杂先天性畸形的致死病例,该病例表现出水致死综合征中描述的多种体征。我们的病例呈现出以下特定特征:巨头畸形、中线唇裂、腭裂、双手和双脚多指畸形,但无枕骨裂,而枕骨裂被认为是该综合征的特征性体征。对HYLS1基因的测序分析未发现芬兰病例中存在的点突变或该基因的其他突变。

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