Single aberrant umbilical artery in a fetus with severe caudal defects: Sirenomelia or caudal dysgenesis

被引:0
|
作者
PerezAytes, A
Montero, L
Gomez, J
Paya, A
机构
[1] HOSP LA FE,DEPT RADIOL,E-46009 VALENCIA,SPAIN
[2] HOSP LA FE,DEPT PATHOL,E-46009 VALENCIA,SPAIN
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 69卷 / 04期
关键词
sirenomelia; caudal dysgenesis; single umbilical artery; postmortem arteriogram;
D O I
10.1002/(SICI)1096-8628(19970414)69:4<409::AID-AJMG14>3.0.CO;2-R
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe a 1,000-g twin fetus with absent kidneys and ureters, anal atresia and minimal evidence of external genitalia, and hypoplastic lower limbs with absent feet. A postmortem arteriogram showed a large single umbilical artery in direct continuation with the abdominal aorta, a unique anomaly almost always related to sirenomelia, We discuss the possible diagnosis of this case as sirenomelia or caudal dysgenesis, and the controversy as to whether they are two related or separate entities. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:409 / 412
页数:4
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