股动脉重复畸形：一例报告

Femoral duplication: a case report.

作者信息

Bodurtha J, Coutinho M, Benator R, Nogi J, Sholley M, Nance W E

机构信息

Department of Human Genetics, Children's Hospital, Medical College of Virginia, Richmond 23298-0033.

出版信息

Am J Med Genet. 1989 Jun;33(2):165-9. doi: 10.1002/ajmg.1320330204.

DOI:10.1002/ajmg.1320330204

PMID:2764024

Abstract

Femoral duplication is a rare anomaly that has been described as an isolated entity and in association with other congenital defects. Since the description by Erlich in 1885, 24 additional cases have been reported. The present report concerns a 34-week black female infant with apparent bilateral femoral duplication associated with a meningocele and abdominal, genitourinary, vertebral, and lower-limb anomalies. The cause is unknown. Femoral duplication is a developmental field defect, hence causally heterogeneous.

摘要

股动脉重复畸形是一种罕见的异常情况，已被描述为一种孤立的病症，并与其他先天性缺陷相关联。自1885年埃利希首次描述以来，又有24例相关病例被报道。本报告涉及一名34周大的黑人女婴，其明显存在双侧股动脉重复畸形，并伴有脑脊膜膨出以及腹部、泌尿生殖系统、脊柱和下肢的异常。病因不明。股动脉重复畸形是一种发育场缺陷，因此病因具有异质性。