Chronic cutaneous candidiasis in children: should we stop there? Report of two cases associated with auto-immune polyendocrinopathy syndrome type I
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 adol...
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2020-03-01T00:00:00Z.
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