Article ID Journal Published Year Pages File Type
2814520 European Journal of Medical Genetics 2006 4 Pages PDF
Abstract

Fibular aplasia–ectrodactyly is a rare disorder of the central axis, characterized by shortening of the affected limbs and formation of split hand and/or foot. Here we report on a severely affected case of fibular aplasia with ectrodactyly, in which the upper limb malformations are more pronounced than usually described in sporadic cases.

Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
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