Autoimmune polyglandular syndrome type I. A case report
The Turkish Journal of Pediatrics, 1997 Autoimmune polyglandular syndrome (APS) type I is a disorder that consists of three primary diseases: hypoparathyroidism (HPT), adrenocortical insufficiency (ACI) and chronic mucocutaneous candidiasis.
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Novel <i>STAT1</i> mutation in a paediatric case of chronic mucocutaneous candidiasis complicated by primary hypothyroidism: clinical presentation, genetic analysis and prognostic implications. [PDF]
BMJ Case Rep, 2023 Hou F, Zhang T, Chen F, Jiang L.
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Chronic primary mucocutaneous candidiasis in a child
Indian Journal of Paediatric Dermatology, 2020 Aastha Gupta +3 more
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IL-17 serum level in patients with chronic mucocutaneous candidiasis disease. [PDF]
Pediatr Allergy Immunol, 2022 Chimenz R +5 more
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Case for diagnosis. Disseminated erythematous and scaly plaques: chronic mucocutaneous candidiasis [PDF]
Anais Brasileiros de Dermatologia, 2023 Nathalia Chebli de Abreu +3 more
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AIRE gene mutation predisposing chronic mucocutaneous candidiasis and pigmented retinitis in two kids from a Chinese family. [PDF]
Emerg Microbes Infect, 2022 Ma Y, Wang X, Li R.
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Three Adult Cases of STAT1 Gain-of-Function with Chronic Mucocutaneous Candidiasis Treated with JAK Inhibitors. [PDF]
J Clin Immunol, 2023 Borgström EW +16 more
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Chronic Mucocutaneous Candidiasis
The Nishinihon Journal of Dermatology, 1975 MATSUMOTO, Tadahiko, HONBO, Shozo
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Co-Occurrence of Chronic Mucocutaneous Candidiasis with Woolly Hair. [PDF]
Skin Appendage Disord, 2021 Gaurav V, Grover C.
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