II型并指（趾）畸形或并指（趾）多指（趾）畸形。
Type II syndactyly or synpolydactyly.
作者信息
De Smet L, Fabry G
机构信息
Department of Orthopedic Surgery, University Hospital Pellenberg, K.U. Leuven, Pellenberg, Belgium.
出版信息
Acta Orthop Belg. 1992;58(2):209-12.
PMID:1321548
Abstract
A family with syndactyly type II or synpolydactyly is described. The autosomal dominant inheritance is confirmed by this pedigree. In combination of this anomaly a brachymesophalangia of the fifth finger was inherited by most family members. The duplicated phalanx was resected and the syndactyly separated in the proband with excellent functional and cosmetic results.
摘要
本文描述了一个患有II型并指（趾）或并指（趾）多指（趾）畸形的家族。该系谱证实了常染色体显性遗传。在这种异常情况中，多数家族成员还遗传了第五指的短中节指骨。对先证者切除了重复的指骨并分离了并指（趾），功能和外观效果极佳。
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