Chronic cutaneous candidiasis in children: should we stop there? Report of two cases associated with auto-immune polyendocrinopathy syndrome type I

BACKGROUND: Auto-immune polyendocrinopathy syndrome type I is a rare genetic disease, usually revealed by chronic superficial candidiasis and autoimmune endocrine dysfunction in childhood. CASES PRESENTATION: We report the cases of 2 children, a 4 years-11 months old boy and 13 years old adolescent,...

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Detalles Bibliográficos
Autores principales: Minka, Basilice Mireille, Sibetcheu T, Aurélie, Sap, Suzanne Ngo Um, Bissa, Maryse Césarine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081563/
https://www.ncbi.nlm.nih.gov/pubmed/32188450
http://dx.doi.org/10.1186/s12887-020-02030-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081563/
https://www.ncbi.nlm.nih.gov/pubmed/32188450
http://dx.doi.org/10.1186/s12887-020-02030-y

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