Autoimmune polyglandular syndrome (APS) type I is a disorder that cons
ists of three primary diseases: hypoparathyroidism (HPT), adrenocortic
al insufficiency (ACI) and chronic mucocutaneous candidiasis. Several
other disorders may be associated. the diagnosis of APS type I was mad
e in a 16-year-old patient with HPT, Hashimato's thyroiditis and ACI i
n our department. She has been observed for more than four years for o
ther possible endocrine and non-endocrine disorders.