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无颌-前脑无裂畸形:一种涉及面部和脑部的发育场复合体。3例报告。

Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases.

作者信息

Bixler D, Ward R, Gale D D

出版信息

J Craniofac Genet Dev Biol Suppl. 1985;1:241-9.

PMID:3932506
Abstract

Agnathia-holoprosencephaly (A-H) is a developmental field complex involving a graded series of defects in the jaws, mouth, tongue, ears, eyes, and brain. Two general groups can be recognized: agnathia with holoprosencephaly (more severe) and agnathia without holoprosencephaly (less severe). This report describes three new cases of agnathia without holoprosencephaly and reviews the recent literature. By combining published cases with those ascertained through a survey of genetic centers in the United States, it appears that there have been at least 24 occurrences of A-H in the past 25 years. An inductive defect of the prechordal mesoderm that also affects neural crest cells is presented as the cause for this developmental field complex. Because of the etiologic heterogeneity associated with developmental field defects, the genetic counselor must provide a wide range of recurrence risks when dealing with the A-H complex.

摘要

无颌-前脑无裂畸形(A-H)是一种发育领域综合征,涉及颌骨、口腔、舌头、耳朵、眼睛和大脑的一系列分级缺陷。可分为两大类:伴有前脑无裂畸形的无颌(更严重)和不伴有前脑无裂畸形的无颌(不太严重)。本报告描述了3例不伴有前脑无裂畸形的无颌新病例,并对近期文献进行了综述。通过将已发表的病例与通过对美国遗传中心的调查确定的病例相结合,在过去25年中似乎至少有24例A-H病例。前索中胚层的诱导缺陷也影响神经嵴细胞,被认为是这种发育领域综合征的病因。由于与发育领域缺陷相关的病因异质性,遗传咨询师在处理A-H综合征时必须提供广泛的复发风险。

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