Focal dermal hypoplasia: Unusual presentation in Saudi Arabia
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...
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Main Authors: | , |
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Format: | Book |
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Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
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Summary: | 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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Item Description: | 2352-2410 10.1016/j.jdds.2015.11.004 |