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[卡彭特综合征]

[Carpenter's syndrome].

作者信息

Piussan C, Van Poperinghe M, Grumbach Y, Audebert M, Helsemans C, Risbourg B

出版信息

Arch Fr Pediatr. 1977 Nov;34(9):891-8.

PMID:606189
Abstract

A newborn boy presented with an acrocephaly characterized by a coronal craniosynostoses, open sagittal sutures and abnormally high and straight forehead. He was the only child of young, unrelated, healthy parents; there was no familial history of dysmorphy. Facial asymmetry was important and associated with posterior cleft palate, syndactylia of the tips and polydactylia of feet, due to a splitting of the first metatarsus. The child also had a congenital heart disease, like in half of the 15 published cases. In older children, mental retardation is usually observed, often associated with obesity and hypogonadism. Polydactylia permitted to exclude Apert's acrocephalosyndactylia in which there is a normal number of finger arms and which seems to be a dominant mutation, while the transmission of Carpenter's syndrome appears autosomal recessive, thus requiring restrictive genetic counselling.

摘要

一名男婴出生时患有尖头畸形,其特征为冠状缝早闭、矢状缝开放以及额头异常高且直。他是一对年轻、无血缘关系且健康的父母的独子;家族中没有畸形病史。面部不对称较为明显,伴有后腭裂、指尖并指以及足部多指(第一跖骨分裂所致)。该患儿还患有先天性心脏病,在已发表的15例病例中有半数存在此情况。在年龄较大的儿童中,通常会观察到智力发育迟缓,且常伴有肥胖和性腺功能减退。多指畸形可排除Apert尖头并指综合征,该病手指数量正常,似乎是显性突变,而 Carpenter 综合征的遗传方式为常染色体隐性遗传,因此需要进行严格的遗传咨询。

相似文献

1
[Carpenter's syndrome].[卡彭特综合征]
Arch Fr Pediatr. 1977 Nov;34(9):891-8.
8
Apert's syndrome: (acrocephalosyndactylism).
J Foot Surg. 1981 Winter;20(4):210-13.

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