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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,...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| 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 |