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伴有胼胝体发育不全的鲁宾斯坦-泰比综合征

Rubinstein-Taybi syndrome with agenesis of corpus callosum.

作者信息

Mishra Shubhankar, Agarwalla Sunil Kumar, Potpalle Dnyaneshwar Ramesh, Dash Nishant Nilotpal

机构信息

Department of Paediatrics, MKCG Medical College, Berhampur, Odisha, India.

出版信息

J Pediatr Neurosci. 2015 Apr-Jun;10(2):175-7. doi: 10.4103/1817-1745.159207.

Abstract

Rubinstein-Taybi syndrome (RSTS) is a rare genetic disorder with characteristic morphological anomaly. Our patient was a 4.5-year-old girl came with features like broad thumbs, downward slanting palpebral fissures and mental retardation. Systemic abnormalities such as repeated infection, seizure with developmental delay were also associated with it. She was having head banging behavior abnormal slurring speech, incoordination while transferring things from one hand to other. Galaxy of clinical pictures and magnetic resonance imaging report helped to clinch the diagnosis as a case of "RSTS with corpus callosal agenesis" which to the best of our knowledge has never been reported in past from India.

摘要

鲁宾斯坦-泰比综合征(RSTS)是一种罕见的遗传性疾病,具有特征性的形态异常。我们的患者是一名4.5岁女孩,有宽拇指、睑裂向下倾斜和智力发育迟缓等特征。反复感染、伴有发育迟缓的癫痫发作等全身性异常也与之相关。她有撞头行为、异常言语含糊不清、双手物品转移时不协调。一系列临床症状和磁共振成像报告有助于确诊为“胼胝体发育不全的RSTS”,据我们所知,印度过去从未有过此类报道。

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