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Unilateral Focal Dermal Hypoplasia (Goltz Syndrome): Case Report and Literature Review
Focal dermal hypoplasia (FDH) or Goltz syndrome is a rare X-linked dominant multisystemic disease involving the ectoderm, mesoderm, and endoderm. About 95% of the cases appear de novo, and 90% of them are females. Recently, the studies revealed that FDH is caused by a mutation in the PORCN gene. We...
Gorde:
| Argitaratua izan da: | Case Rep Dermatol |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
S. Karger AG
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5981586/ https://ncbi.nlm.nih.gov/pubmed/29867430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000488521 |
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