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卡彭特综合征:两例同胞病例报告。

Carpenter syndrome: report of two siblings.

作者信息

Işlek I, Küçüködük S, Incesu L, Selçuk M B, Aygün D

机构信息

Ondokuz Mayis University, School of Medicine, Department of Pediatrics, Samsun, Turkey.

出版信息

Clin Dysmorphol. 1998 Jul;7(3):185-9.

PMID:9689991
Abstract

Carpenter syndrome consists of acrocephaly, soft tissue syndactyly, short fingers, preaxial polydactyly, congenital heart disease, hypogenitalism, cryptorchidism, obesity, umbilical hernia and mental retardation. Here we report two affected sibs (IQs were 80 and 93) presenting various cerebrospinal malformations, i.e. frontal lobe deformity, narrowed foramen magnum, hypoplastic posterior fossa, kinked spinal cord, and syrinx cavitation demonstrated by magnetic resonance imaging.

摘要

Carpenter综合征包括尖头畸形、软组织并指畸形、短指、轴前多指畸形、先天性心脏病、生殖器发育不全、隐睾、肥胖、脐疝和智力发育迟缓。在此,我们报告两名患病同胞(智商分别为80和93),他们存在各种脑脊髓畸形,即额叶畸形、枕骨大孔狭窄、后颅窝发育不全、脊髓扭曲和磁共振成像显示的脊髓空洞症。

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