Autoimmune polyglandular syndrome type I - A case report

Cinaz P., Bideci A., Haznedaroglu A., Ezgu F. S., Agaoglu O., Kursaklioglu S.

TURKISH JOURNAL OF PEDIATRICS, cilt.39, sa.2, ss.271-275, 1997 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 39 Sayı: 2
  • Basım Tarihi: 1997
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.271-275
  • Anahtar Kelimeler: autoimmune, polyglandular syndrome type I, childhood, DISEASE, FAILURE
  • Gazi Üniversitesi Adresli: Evet

Özet

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