Iyer Prasad, Smith Rupert
Department of Paediatrics, Rochdale Infirmary, Whitehall street, Rochdale, Lancs OL12 0NB.
Clin Dysmorphol. 2005 Apr;14(2):101-103.
We describe a further patient with cranio-cerebellar-cardiac or 3C syndrome. She presented with the characteristic features of Dandy-Walker malformation of the brain, congenital cardiac defect, dysmorphic facies and post-natal growth failure. She had gastro-oesophageal reflux and severe feeding difficulties which are still present at the age of four years. Despite her numerous medical problems, she is demonstrating near-normal development. Feeding difficulties appear to be a prominent feature of the 3C syndrome.
我们描述了另一例患有颅-小脑-心脏或3C综合征的患者。她表现出脑Dandy-Walker畸形、先天性心脏缺陷、面部畸形和出生后生长发育迟缓的特征性表现。她有胃食管反流和严重的喂养困难,这些问题在4岁时仍然存在。尽管她有许多健康问题,但她的发育接近正常。喂养困难似乎是3C综合征的一个突出特征。