UPDATE ON A FAMILY WITH HAND FOOT GENITAL SYNDROME - HYPOSPADIAS AND URINARY-TRACT ABNORMALITIES IN 2 BOYS FROM THE 4TH GENERATION

被引:19
作者
DONNENFELD, AE [1 ]
SCHRAGER, DS [1 ]
CORSON, SL [1 ]
机构
[1] PENN HOSP,DEPT OBSTET & GYNECOL,REPROD ENDOCRINOL SECT,PHILADELPHIA,PA 19107
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 04期
关键词
HAND FOOT GENITAL SYNDROME; MULLERIAN ANOMALY; HYPOSPADIAS; URINARY TRACT;
D O I
10.1002/ajmg.1320440419
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe a fourth generation of involvement with hand-foot-genital syndrome. The first 3 generations of this family, which included 5 affected females and no affected males, were reported previously by Verp et al. [1983]. In the fourth generation, 2 affected males are identified. To our knowledge, the findings of bilateral vesicoureteral reflux in one boy and bilateral ureteropelvic junction obstruction in his cousin represent the first reports of urinary tract abnormalities in males with this syndrome.
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页码:482 / 484
页数:3
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