Tarhan Erkan, Oğuz Haldun, Safak Mustafa Asim, Samim Erdal
Ministry of Health, Ankara Training and Research Hospital, Clinic of Otolaryngology, Ankara, Turkey.
Int J Pediatr Otorhinolaryngol. 2004 Mar;68(3):353-7. doi: 10.1016/j.ijporl.2003.10.009.
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.
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。