Congenital incomplete duplication of lower extremity (polymelia) accompanied with anorectal malformation and unilateral deafness-Reference-Cited by-同舟云学术

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Congenital incomplete duplication of lower extremity (polymelia) accompanied with anorectal malformation and unilateral deafness

Published:2024-06-24 Issue:7 Volume:12 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Shinden Yumetaka¹,Hakozaki Michiyuki¹²^ORCID,Hiruta Shun³,Tanaka Hideaki⁴^ORCID,Matsumoto Yoshihiro¹

Affiliation:

1. Department of Orthopaedic Surgery Fukushima Medical University School of Medicine Fukushima Japan

2. Higashi‐Shirakawa Orthopaedic Academy Fukushima Medical University School of Medicine Fukushima Japan

3. Department of Pediatrics Fukushima Medical University School of Medicine Fukushima Japan

4. Department of Pediatric Surgery Fukushima Medical University Hospital Fukushima Japan

Abstract

Key Clinical MessagePolymelia (supernumerary limbs) is an extremely rare congenital condition in humans. Because congenital anorectal malformation is a relatively common complication of polymelia and it may require emergency surgery as in the present case, accompanying malformations must be investigated.

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.9119

Reference3 articles.

1. Congenital duplication of lower extremity – A case report and review of the literature

2. Prenatal ultrasound‐based diagnosis of fetal OEIS complex associated with lower limb polymelia and cardiac, hepatic dysplasia: A case report

3. A Rare Sonographic Case of Caudal Duplication Versus Polymelia

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