Salmon M A, Wakefield M A
Dev Med Child Neurol. 1977 Aug;19(4):521-4. doi: 10.1111/j.1469-8749.1977.tb07948.x.
A nine-year-old girl with symmetrical acral deformities and anomalies of the renal tract is described. There have been four previous reports of this association, all in phenotypic males. In each case there was moderate intellectual retardation and in two cases dermatoglyphic analysis revealed abnormalities. It is suggested that there is now sufficient evidence to give the acro-renal syndrome independent status.
本文描述了一名患有对称性肢端畸形和泌尿道异常的9岁女孩。此前已有4篇关于这种关联的报道，所有病例均为表型男性。在每个病例中均存在中度智力发育迟缓，2例病例的皮纹分析显示异常。目前认为，现有足够证据赋予肢端-肾脏综合征独立疾病地位。
