PRENATAL-DIAGNOSIS OF WEYERS SYNDROME (DEFICIENT ULNAR AND FIBULAR RAYS WITH BILATERAL HYDRONEPHROSIS)

被引：11

作者：

ELEJALDE, BR

DEELEJALDE, MM

BOOTH, C

KAYE, C

HOLLISON, L

机构：

[1] UNIV WISCONSIN, MT SINAI MED CTR,SCH MED,DEPT OBSTET & GYNECOL, GENET SECT, MILWAUKEE CLIN CAMPUS, MILWAUKEE, WI 53201 USA

[2] UNIV WISCONSIN, MT SINAI MED CTR, DEPT INTERNAL MED, MILWAUKEE, WI 53201 USA

[3] UNIV WISCONSIN, MT SINAI MED CTR, DEPT MED GENET, MILWAUKEE, WI 53201 USA

[4] LUTHERAN GEN HOSP, PARK RIDGE, IL 60068 USA

[5] UNIV WISCONSIN, SCH NURSING, MILWAUKEE, WI 53201 USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1985年 / 21卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320210305

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A fetus with Weyers oligodactyly was studied after a previous sibling had been born with that condition. Prenatal diagnosis was undertaken using ultrasound to visualize the long bones, which were severely affected by the condition at 19 wk of gestation. Most notable were the ulnae and fibulae, which were very short; the fetus had bilateral hydronephrosis.

引用

页码：439 / 444

页数：6

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