KLICK Syndrome Linked to a POMP Mutation Has Features Suggestive of an Autoinflammatory Keratinization Disease

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK) syndrome is a rare autosomal recessive skin disorder characterized by palmoplantar keratoderma, linear hyperkeratotic plaques, ichthyosiform scaling, circular constrictions around the fingers, and numerous papules distri...

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Detalles Bibliográficos
Autores principales: Takeichi, Takuya, Akiyama, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203212/
https://www.ncbi.nlm.nih.gov/pubmed/32425927
http://dx.doi.org/10.3389/fimmu.2020.00641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203212/
https://www.ncbi.nlm.nih.gov/pubmed/32425927
http://dx.doi.org/10.3389/fimmu.2020.00641

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