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

Abstract:

: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.

journal_name

Arch Gynecol Obstet

authors

Zanforlin Filho SM,Guimarães Filho HA,Araujo Júnior E,Pires CR,Mattar R,Nardozza LM

doi

10.1007/s00404-006-0250-z

subject

Has Abstract

pub_date

2007-04-01 00:00:00

pages

315-6

issue

4

eissn

0932-0067

issn

1432-0711

journal_volume

275

pub_type

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