| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3214710 | Journal of Dermatology & Dermatologic Surgery | 2016 | 5 Pages |
Abstract
Focal dermal hypoplasia (Goltz syndrome) is a rare genetic multisystem characterized by multiple abnormalities of ectodermal and mesodermal origin. It is found predominantly in females. We report a case of a two month-old baby girl who had dermal hypoplasia, atrophic skin lesions with telangiectasia in a linear pattern, fat herniations, papillomas and cleft of the upper lip, ectrodactyly, claw hands, microphthalmia and unusual association of gastrointestinal omphalocele.
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Authors
Awadh Alamri, Mazin Al Jabri,