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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...
Autores principales: | Dai, Yuwei, Zheng, Xiaodong, Zhang, Qi, Hu, Xia, Wang, Peiguang, Yang, Sen |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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 |
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