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Updated: Aug 11, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Fibular aplasia with ectrodactyly--broadening the clinical spectrum
D Gieruszczak-Bialek1, M Oldak, A Skorka
1Department of Diabetology, Neonatology and Birth Defects, Warsaw Medical University, Dzialdowska 1, PL-01-184, Warsaw, Poland.
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.
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