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Focal Dermal Hypoplasia: A Rare Case Report
Focal dermal hypoplasia (Goltz syndrome) is a rare genetic multisystem disorder primarily involving the skin, skeletal system, eyes, and face. We report the case of an eight-month-old female child who presented with multiple hypopigmented atrophic macules along the lines of blaschko, skeletal anomal...
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| Publicat a: | Indian J Dermatol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4318042/ https://ncbi.nlm.nih.gov/pubmed/25657436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.147876 |
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