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...

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Detalles Bibliográficos
Autores principales: Tenkir, Addis, Teshome, Samuel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case Report
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

Internet

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

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