Suppr超能文献

木匠综合征表型

The carpenter syndrome phenotype.

作者信息

Tarhan Erkan, Oğuz Haldun, Safak Mustafa Asim, Samim Erdal

机构信息

Ministry of Health, Ankara Training and Research Hospital, Clinic of Otolaryngology, Ankara, Turkey.

出版信息

Int J Pediatr Otorhinolaryngol. 2004 Mar;68(3):353-7. doi: 10.1016/j.ijporl.2003.10.009.

Abstract

Carpenter syndrome (Acrocephalopolysyndactyly type II), first described in 1901, consists of acrocephaly, syndactyly, polydactyly, congenital heart disease, mental retardation, hypogenitalism, cryptorchidism, obesity, umbilical hernia and bony abnormalities. We report a 6 years old boy presenting as a union of these malformations and also having bilateral sensorineural hearing loss. Auditory disturbances are not common among Carpenter syndrome patients. According to our knowledge, this is the first Carpenter syndrome case whose hearing loss is demonstrated by auditory brainstem response (ABR) test.

摘要

卡彭特综合征(II型尖头并指多指畸形)于1901年首次被描述,其特征包括尖头畸形、并指(趾)、多指(趾)、先天性心脏病、智力发育迟缓、生殖功能减退、隐睾、肥胖、脐疝和骨骼异常。我们报告了一名6岁男孩,他合并了这些畸形,并且还患有双侧感音神经性听力损失。听觉障碍在卡彭特综合征患者中并不常见。据我们所知,这是首例通过听性脑干反应(ABR)测试证实存在听力损失的卡彭特综合征病例。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验