卡米综合征并发咽食管穿孔。
Carmi syndrome complicated by pharyngo-esophageal perforation.
作者信息
Sarin Y K, Nagdeve N G
机构信息
Department of Pediatric Surgery, Maulana Azad Medical College, New Delhi 110 002, India.
出版信息
Indian Pediatr. 2006 Jan;43(1):61-4.
PMID:16465009
Abstract
We describe a neonate having congenital pyloric atresia (CPA) associated with epidermolysis bullosa (EB), also known as Carmi syndrome. The case is unusual as it was complicated with pharyngo-esophageal perforation (PEP) and a definite family history of EB in pervious generations could be recorded.
摘要
我们描述了一名患有先天性幽门闭锁（CPA）并伴有大疱性表皮松解症（EB）（也称为卡米综合征）的新生儿。该病例不同寻常，因为它并发了咽食管穿孔（PEP），并且可以记录到前几代有明确的EB家族史。
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