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

页码：315 / 316

页数：1

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