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Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report
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, faci...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996349/ https://www.ncbi.nlm.nih.gov/pubmed/21092077 http://dx.doi.org/10.1186/1471-2415-10-28 |