Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2814520 | European Journal of Medical Genetics | 2006 | 4 Pages |
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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Authors
D. Gieruszczak-Bialek, M. Oldak, A. Skorka, J. Waligora, L. Korniszewski,