Autoimmune polyglandular syndrome type I. A case report.

@article{Cinaz1997AutoimmunePS,
  title={Autoimmune polyglandular syndrome type I. A case report.},
  author={Peyami Cinaz and Aysun Bideci and A Haznedaroğlu and Fatih S{\"u}heyl Ezg{\"u} and O Ağaoğlu and S K{\"u}rşaklioğlu},
  journal={The Turkish journal of pediatrics},
  year={1997},
  volume={39 2},
  pages={271-5}
}
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… CONTINUE READING