Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report

Abstract

BACKGROUND Goltz syndrome or focal dermal hypoplasia (FDH) is an uncommon multisystem disorder. Herein, we report a typical case of FDH with unilateral ocular, cutaneous and skeletal features. CASE PRESENTATION a 4-year-old girl presented with microphthalmos and iris coloboma of the left eye, facial asymmetry, and a low-set protruding ear. Cutaneous… (More)
DOI: 10.1186/1471-2415-10-28

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Cite this paper

@inproceedings{Tenkir2010GoltzS, title={Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report}, author={Addis Tenkir and Samuel Teshome}, booktitle={BMC ophthalmology}, year={2010} }