首页> 外文期刊>American journal of medical genetics, Part A >A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia.
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A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia.

机译:一种新型的致命小头畸形,具有简化的回旋型和脑干发育不全。

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摘要

We report on four patients from the same family affected by a lethal form of autosomal recessive microcephaly of prenatal onset. Symptoms include low birth-weight and length with disproportionately small head, fetal distress, apnea, seizures and facial features reminiscent of Amish microcephaly and Bowen-Conradi syndrome. Brain imaging revealed a simplified gyral pattern with normal to slightly thinned cortical gray matter, thin corpus callosum, mild brainstem and cerebellar hypoplasia. No abnormalities of the internal organs, eye, or skeleton, and no striking dysmorphic facial features were found to be associated with this syndrome. All patients died within hours to weeks after birth following severe apnea attacks and central hypoventilation. Recessive primary microcephaly with lethality in early infancy is rarely reported. The patients described here do not resemble any other published cases of such clinical severity and the locus for the only reported early lethal microcephaly gene found in Amish families was excluded. Therefore, this appears to be a distinct genetic cause of lethal microcephaly.
机译:我们报告了来自同一个家庭的四名患者受到了产前发作的常染色体隐性小头畸形的致死形式的影响。症状包括出生体重低,身长矮,头部偏小,胎儿窘迫,呼吸暂停,癫痫发作和面部特征,使人联想到阿米什人小头畸形和Bowen-Conradi综合征。脑部影像学检查显示出简单的回肠型,皮层灰质正常至稍变薄,call体变薄,脑干轻度和小脑发育不全。没有发现内部器官,眼睛或骨骼异常,也没有明显的畸形面部特征与该综合征相关。所有患者在出生后数小时至数周内均死于严重的呼吸暂停发作和中枢通气不足。婴儿早期致死性隐性原发性小头畸形的报道很少。此处描述的患者与此类临床严重程度的任何其他已发表病例均不相似,并且排除了在阿米什人家庭中发现的唯一报告的早期致死性小头畸形基因的基因座。因此,这似乎是致死性小头畸形的独特遗传原因。

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