Cargando…

Case Report: Challenges in the Diagnosis of a Case of Mal de Meleda and a Therapeutic Attempt of Ixekizumab and Adalimumab

BACKGROUND: Mal de Meleda (MDM, OMIM 248300) is an autosomal recessive disease characterized by symmetrical and progressive palmoplantar hyperkeratosis soon after birth. Mutations in SLURP1 gene could lead to MDM. Clinically, MDM is easily misdiagnosed as other types of keratoderma due to phenotypic...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Yuwei, Zheng, Xiaodong, Zhang, Qi, Hu, Xia, Wang, Peiguang, Yang, Sen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961326/
https://www.ncbi.nlm.nih.gov/pubmed/35360724
http://dx.doi.org/10.3389/fmed.2022.821301