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全前脑畸形的胚胎发生

Embryogenesis of holoprosencephaly.

作者信息

Shiota Kohei, Yamada Shigehito, Komada Munekazu, Ishibashi Makoto

机构信息

Congenital Anomaly Research Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.

出版信息

Am J Med Genet A. 2007 Dec 15;143A(24):3079-87. doi: 10.1002/ajmg.a.32020.

Abstract

Holoprosencephaly (HPE) is a malformation of the human brain caused primarily by incomplete division of the prosencephalon into two halves and is often associated with various facial anomalies. Although HPE is rather rare in newborns (1/10,000-15,000 births), it is frequently encountered in therapeutic abortuses (>1/250). To date, nine gene mutations responsible for human HPE have been identified, but the pathogenetic mechanisms of the craniofacial anomalies in HPE have just begun to be understood. Here, we summarize our studies on human embryos with HPE and discuss the embryogenesis and the underlying molecular mechanisms of HPE malformations under the following headings: pathology, pathogenesis, and critical period of development.

摘要

前脑无裂畸形(HPE)是一种人类脑部畸形,主要由前脑未完全分裂成两半所致,常伴有各种面部异常。虽然HPE在新生儿中相当罕见(每10000 - 15000例出生中有1例),但在治疗性流产中却经常出现(超过1/250)。迄今为止,已鉴定出9种导致人类HPE的基因突变,但HPE中颅面异常的发病机制才刚刚开始被了解。在此,我们总结了对患有HPE的人类胚胎的研究,并在以下标题下讨论HPE畸形的胚胎发生及潜在分子机制:病理学、发病机制和发育关键期。

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