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首页> 外文期刊>Clinical dysmorphology >A new case of VACTERL association with congenital arachnoid cyst
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A new case of VACTERL association with congenital arachnoid cyst

机译:VACTERL合并先天性蛛网膜囊肿的新病例

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Introduction:VACTERL association is characterized by V-vertebral anomaly, A-anal atresia, C-cardiac anomaly, T-tracheo-oesophageal fistula, E-oesophageal atresia, R-renal anomaly and L-limb anomaly. Three, or in some reports two, of seven anomalies are sufficient to establish the diagnosis of VACTERL (Shaw-Smith, 2006). Brain malformations and hydrocephalus have been observed in some patients with VACTERL association referred to as VACTERL-H (Balci et al., 2003; Vatansever et a/., 2004). In this study, we report a female newborn with VACTERL association and arachnoid cyst localized in the right Sylvian fissure, ventriculomegaly and agenesis of the corpus callosum. This association has not been reported earlier
机译:简介:VACTERL关联的特征是V型椎骨异常,A型肛门闭锁,C型心脏异常,T型气管食管瘘,E型食管闭锁,R型肾异常和L型肢异常。七个异常中的三个,或者在某些报告中,两个,足以确定VACTERL的诊断(Shaw-Smith,2006年)。在一些与VACTERL相关的患者中发现了脑畸形和脑积水,称为VACTERL-H(Balci等,2003; Vatansever等,2004)。在这项研究中,我们报告了一名女性,其新生儿患有VACTERL关联,蛛网膜囊肿位于右侧的Sylvian裂隙,脑室肥大和the体发育不全。此关联尚未被报道

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