Lahiri Anindya, Lester Ruth
Birmingham Children's Hospital, Birmingham, UK.
J Plast Reconstr Aesthet Surg. 2009 Apr;62(4):462-5. doi: 10.1016/j.bjps.2007.11.036. Epub 2008 Jan 2.
Russell Silver syndrome (RSS) is a genetic disorder of unknown aetiology. The disorder is clinically and genetically heterogeneous, and various modes of inheritance and genetic abnormalities have been described. A large number of clinical features are associated with this condition. Growth retardation, typical facies, limb asymmetry, delayed bony growth and clinodactyly are some of the most constant features of RSS. We report a small series of patients presenting with a range of hand anomalies, some of which have not been previously reported in association with this condition.
罗素 - 西尔弗综合征(RSS)是一种病因不明的遗传性疾病。该疾病在临床和遗传方面具有异质性,并且已经描述了多种遗传模式和基因异常情况。许多临床特征与这种病症相关。生长发育迟缓、典型面容、肢体不对称、骨骼生长延迟和小指内弯是RSS最常见的一些特征。我们报告了一小系列呈现各种手部异常的患者,其中一些异常此前尚未见与该病症相关的报道。