无波特综合征的并腿畸形：磁共振成像特征

Sirenomelia without Potter syndrome: MR characteristics.

作者信息

Savader S J, Savader B L, Clark R A

机构信息

Department of Radiology, University of South Florida College of Medicine, Tampa 33612.

出版信息

J Comput Assist Tomogr. 1989 Jul-Aug;13(4):689-91. doi: 10.1097/00004728-198907000-00027.

DOI:10.1097/00004728-198907000-00027

PMID:2745791

Abstract

Sirenomelia is a rare birth defect characterized by fusion of the lower extremities into one limb and a wide spectrum of both genitourinary and lower gastrointestinal tract anomalies. We wish to report the occurrence of this syndrome in an infant whose genitourinary and gastrointestinal anomalies are compatible with life.

摘要

并腿畸形是一种罕见的出生缺陷，其特征为下肢融合成一条肢体，并伴有广泛的泌尿生殖系统和下胃肠道异常。我们希望报告该综合征在一名泌尿生殖系统和胃肠道异常但可存活婴儿中的发生情况。