AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE-I - A CASE-REPORT

Citation
P. Cinaz et al., AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE-I - A CASE-REPORT, Turkish Journal of Pediatrics, 39(2), 1997, pp. 271-275
Citations number
11
Categorie Soggetti
Pediatrics
ISSN journal
00414301
Volume
39
Issue
2
Year of publication
1997
Pages
271 - 275
Database
ISI
SICI code
0041-4301(1997)39:2<271:APST-A>2.0.ZU;2-7
Abstract
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.