Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab

Lamellar ichthyosis (LI) is a rare autosomal cornification disorder, with most cases due to a mutation in the transglutaminase-1 (TGM1) gene on chromosome 14. Patients with LI usually present with a collodion membrane and mild erythroderma at birth, with the collodion membranes shedding within the f...

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Detalles Bibliográficos
Autores principales: Binkhonain, Faisal K, Aldokhayel, Sara, BinJadeed, Hessah, Madani, Abdulaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236574/
https://www.ncbi.nlm.nih.gov/pubmed/35769328
http://dx.doi.org/10.2147/BTT.S362391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236574/
https://www.ncbi.nlm.nih.gov/pubmed/35769328
http://dx.doi.org/10.2147/BTT.S362391

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