Su Pen-Hua, Chen Jia-Yuh, Chen Suh-Jen, Yang Kai-Chi
Department of Pediatrics, Division of Neonatology, Chung Shan Medical University Hospital, Taichung, Taiwan.
Pediatr Neonatol. 2008 Jun;49(3):88-93. doi: 10.1016/S1875-9572(08)60019-4.
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.
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。