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无牙症作为裂指(趾)-外胚层发育不良-唇裂(EEC)综合征的唯一临床体征。

Anodontia as the sole clinical sign of the ectrodactyly-ectodermal dysplasia-cleft lip (EEC) syndrome.

作者信息

Chranowska K H, Krajewska-Walasek M, Rump Z, Wisniewski L, Fryns J P

机构信息

Department of Human Genetics, Child Health-Centre Memorial Hospital, Warsaw.

出版信息

Genet Couns. 1990;1(1):67-73.

PMID:2222925
Abstract

In this report we present another family with oligosymptomatic expression of the EEC syndrome. A mother with complete absence of the permanent teeth had two children with split hand/split foot deformity, as typically seen in the EEC syndrome. Cleft lip/cleft palate was also present in one of them. The great variability in expression of this autosomal dominant syndrome is discussed and the difficulties in genetic counseling are emphasized.

摘要

在本报告中,我们介绍了另一例EEC综合征表现为症状较少的家族病例。一位恒牙完全缺失的母亲育有两个孩子,他们患有典型的EEC综合征所具有的并指/并趾畸形。其中一个孩子还患有唇腭裂。本文讨论了这种常染色体显性综合征表现的巨大变异性,并强调了遗传咨询中的困难。

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