Suppr超能文献

6号染色体长臂末端缺失

Terminal deletion of chromosome 6q.

作者信息

Su Pen-Hua, Chen Jia-Yuh, Chen Suh-Jen, Yang Kai-Chi

机构信息

Department of Pediatrics, Division of Neonatology, Chung Shan Medical University Hospital, Taichung, Taiwan.

出版信息

Pediatr Neonatol. 2008 Jun;49(3):88-93. doi: 10.1016/S1875-9572(08)60019-4.

Abstract

Terminal deletions of chromosome 6q are rare. Clinical features associated with 6q terminal deletion syndrome include psychomotor retardation, seizures, hypotonia, short neck, and facial abnormalities, as well as various case-specific anomalies. Here, we describe a girl with 6q terminal deletion syndrome and unusually short stature. Features of previously described patients are also summarized.

摘要

6号染色体长臂末端缺失很少见。与6q末端缺失综合征相关的临床特征包括精神运动发育迟缓、癫痫发作、肌张力减退、颈部短和面部异常,以及各种特定病例的异常情况。在此,我们描述一名患有6q末端缺失综合征且身材异常矮小的女孩。还总结了先前报道患者的特征。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验