A 20-year study of autoimmune polyendocrine syndrome type II and III in Taiwan

Tseng, Hsu-HuaHsu-HuaTsengLin, Yen-BoYen-BoLinLin, Kuan-YuKuan-YuLinCHIA-HUNG LINHUNG-YUAN LICHIA-HSUIN CHANGYI-CHING TUNGPEI-LUNG CHENCHIH-YUAN WANGWEI-SHIUNG YANGSHYANG-RONG SHIH2024-01-082024-01-082023-12-012235-0802https://scholars.lib.ntu.edu.tw/handle/123456789/638248Autoimmune polyendocrine syndrome (APS) is a rare immune-endocrinopathy characterized by the failure of at least two endocrine organs. Clinical characteristics have mainly been described in the Western population. This study comprehensively analyzed the demographic and clinical manifestations of APS II and APS III in Taiwan.enanti-parietal cell antibody; autoimmune polyendocrine syndrome; autoimmune thyroid disease; primary adrenal insufficiency; type 1 diabetes mellitus[SDGs]SDG3A 20-year study of autoimmune polyendocrine syndrome type II and III in Taiwanjournal article10.1530/ETJ-23-0162378784162-s2.0-85179764392https://api.elsevier.com/content/abstract/scopus_id/85179764392