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腭裂、羊膜带和多指畸形:一种独特的表型,支持羊膜带序列的内在机制。

Clefting, amniotic bands, and polydactyly: a distinct phenotype that supports an intrinsic mechanism for amniotic band sequence.

作者信息

Robin Nathaniel H, Franklin Judith, Prucka Sandra, Ryan Ashley B, Grant John H

机构信息

Department of Genetics, University of Alabama at Birmingham, 35294-0024, USA.

出版信息

Am J Med Genet A. 2005 Sep 1;137A(3):298-301. doi: 10.1002/ajmg.a.30885.

Abstract

Amniotic band sequence (ABS) is a well-described condition involving a variety of congenital anomalies in association with fibrous bands. However, many cases are associated with birth defects that are not readily explained by the mechanism of fibrous strings entangling body parts and causing disruption of the fetal structures. The most common of these is typical cleft lip and palate (CLP). Here we describe such a case, with typical ABS limb defects and constriction bands, along with CLP, supernumerary left nipple, polydactyly, and a skin papilla. This case is nearly identical to a child previously described by Guion-Almieda and Richieri-Costa [2000] and may, therefore, represent a previously unrecognized syndrome that overlaps with ABS. Furthermore it may be that cases with ABS-like anomalies associated with CLP represent a different condition, possibly caused by mutations in the genes Disorganization, p63, or IRF6.

摘要

羊膜带序列(ABS)是一种已被充分描述的病症,涉及与纤维带相关的多种先天性异常。然而,许多病例伴有出生缺陷,而纤维束缠绕身体部位并导致胎儿结构破坏的机制并不能轻易解释这些缺陷。其中最常见的是典型的唇腭裂(CLP)。在此,我们描述这样一例病例,伴有典型的ABS肢体缺陷和束带,以及CLP、左侧多余乳头、多指畸形和一个皮肤乳头。该病例与Guion - Almieda和Richieri - Costa [2000]先前描述的一名儿童几乎完全相同,因此可能代表一种先前未被认识到的与ABS重叠的综合征。此外,可能与CLP相关的类似ABS异常的病例代表一种不同的病症,可能由Disorganization、p63或IRF6基因的突变引起。

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