Novel variants of MEFV and NOD2 genes in familial hidradenitis suppurativa: A case report

We report a two-generation Canadian family of Armenian ancestry with hidradenitis suppurativa where novel mutations in MEVF and NOD2 genes were identified. The father and both children shared a mild-to-moderate hidradenitis suppurativa phenotype together with the features of follicular occlusion (e....

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Detalles Bibliográficos
Autores principales: Jfri, Abdulhadi, Litvinov, Ivan V, Netchiporouk, Elena, O’Brien, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
JCMS Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522817/
https://www.ncbi.nlm.nih.gov/pubmed/33029352
http://dx.doi.org/10.1177/2050313X20953113

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522817/
https://www.ncbi.nlm.nih.gov/pubmed/33029352
http://dx.doi.org/10.1177/2050313X20953113

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