Abstract:
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 auto-immune polyendocrine syndrome type 1. CONCLUSION:The occurrence of chronic cutaneous candidiasis in a child should always imply endocrine screening, to exclude auto-immune polyendocrine syndrome type I.
journal_name
BMC Pediatrjournal_title
BMC pediatricsauthors
Minka BM,Sibetcheu T A,Sap SNU,Bissa MCdoi
10.1186/s12887-020-02030-ysubject
Has Abstractpub_date
2020-03-18 00:00:00pages
128issue
1issn
1471-2431pii
10.1186/s12887-020-02030-yjournal_volume
20pub_type
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