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Article

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

BMC pediatrics - 18 Mar 2020

Minka Basilice Mireille, Sibetcheu T Aurélie, Sap Suzanne Ngo Um, Bissa Maryse Césarine

Abstract excerpt

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, admitted and followed up in the endocrinology unit of the Mother and Child Centre of Chantal Biya's Foundation for...

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Identifiers

PMID: 32188450
DOI: 10.1186/s12887-020-02030-y
PMCID: PMC7081563

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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