一名新生儿患缺指（趾）畸形的病例。

A case of ectrodactyly in a neonate.

作者信息

Kalathia Mitul B, Seta Avani A, Parmar Parin N

机构信息

Department of Pediatrics, PDU Medical College, Rajkot, Gujarat, India.

出版信息

J Clin Neonatol. 2013 Jul;2(3):151-2. doi: 10.4103/2249-4847.120013.

DOI:10.4103/2249-4847.120013

PMID:24251264

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3830155/

Abstract

Ectrodactyly also known as Split hand/foot malformation is a rare limb malformation with autosomal dominant in heritance with variable penetrance, commonly known as "lobster claw hand". Usually it involves midline clefts of the hands and feet with syndactyly. We report a neonate with ectrodactyly and brief review of literature of condition.

摘要

缺指（趾）畸形也称为裂手/裂足畸形，是一种罕见的肢体畸形，呈常染色体显性遗传，外显率可变，通常称为“龙虾爪手”。通常它涉及手和脚的中线裂以及并指（趾）畸形。我们报告了一名患有缺指（趾）畸形的新生儿，并对该病症的文献进行简要回顾。