Sirenomelia sequence: Early prenatal diagnosis of one rare case associated with acardiac malformation

被引：5
|
作者：
Zanforlin Filho S.M. [1 ]
Guimarães Filho H.A. [2 ,3 ]
Araujo Jr. E. [1 ,2 ]
Pires C.R. [1 ,2 ]
Mattar R. [2 ]
Nardozza L.M.M. [2 ]
机构：
[1] Ultrasound Training Center of Sao Paulo (CETRUS), São Paulo
[2] Department of Obstetrics, Sao Paulo's Federal University (Unifesp/EPM), Sao Paulo
[3] CEP 58038-300 João Pessoa, PB, R. R. T. de Melo, 142
来源：
Archives of Gynecology and Obstetrics | 2007年 / 275卷 / 4期
关键词：
Acardiac malformation; Prenatal diagnosis; Sirenomelia;
D O I：
10.1007/s00404-006-0250-z
中图分类号：
学科分类号：
摘要：
Sirenomelia sequence is a very rare congenital malformation, with incidence of around 1.5-4.2 per 100,000 births. Prenatal diagnosis of sirenomelia in the first trimester is rare; there are only five cases reported for the present, and the association of sirenomelia with acardiac malformation is even rarer. We present a rare case of sirenomelia associated with acardiac malformation detected in the first trimester through combined two-dimensional, three-dimensional and color Doppler sonographies. © 2006 Springer-Verlag.
引用
收藏
页码：315 / 316
页数：1
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