Stratton R F, Tolworthy J A, Young R S
South Texas Genetics Center, San Antonio, Texas 78229.
Am J Med Genet. 1994 Jun 1;51(2):153-5. doi: 10.1002/ajmg.1320510215.
We report on a 5-month-old girl with widely spaced nipples, redundant nuchal skin, coarctation of the aorta, anal atresia with distal fistula, postnatal growth retardation, hypotonia, and sparse scalp hair. Initial clinical assessment suggested the diagnosis of Ullrich-Turner syndrome. Chromosome analysis showed a 46,XX,del(2)(q37) karyotype in peripheral lymphocytes. We compare her findings to those of other reported patients with terminal deletions of 2q.
我们报告了一名5个月大的女孩,其乳头间距宽、颈部皮肤冗余、主动脉缩窄、肛门闭锁伴远端瘘管、出生后生长发育迟缓、肌张力减退以及头皮毛发稀疏。初步临床评估提示诊断为乌尔里希-特纳综合征。染色体分析显示外周血淋巴细胞的核型为46,XX,del(2)(q37)。我们将她的检查结果与其他报道的2号染色体长臂末端缺失患者的结果进行了比较。