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Type 1 Segmental Darier Disease: Case Report and Discussion of the Treatment Options
Darier disease is a rare type of autosomal dominant genodermatosis, and it is caused by a mutation in the gene coding for the endoplasmic reticulum membrane calcium pump Ca(2+)-ATPase type 2, leading to compromised intercellular adhesion. Moreover, this condition is characterized by multiple keratot...
Guardat en:
| Publicat a: | Case Rep Dermatol |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
S. Karger AG
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7548966/ https://ncbi.nlm.nih.gov/pubmed/33082742 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000509177 |
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