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- W581102801 abstract "Autoimmune polyglandular syndrome is a group of disorders in which multiple endocrine glands secrete insufficient or excess amounts of hormones. Signs and symptoms depend on which glands are affected. Three types: type I, type II, also known as Schmidt syndrome and type III have been described. The 3 major components of PGA-I are chronic mucocutaneous candidiasis, hypoparathyroidism, and autoimmune adrenal insufficiency. We present the case of a 15 year-old girl admitted to our emergency service with convulsion and carpopedal spasm. Physical examination except heliotropic rash was normal. Laboratory findings were: hypocalcemia-5.8 mg/dl, hyperphosphatemia-11.9 mg/dl, low serum PTH level-5.57 pg/ml(N: 15-65 pg/ml), low 25(OH)D3-10,3 ng/ml (Normal: 19-57,6 ng/ml), antithyroglobulin antibodies 75IU/ml(N:" @default.
- W581102801 created "2016-06-24" @default.
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- W581102801 date "2008-05-01" @default.
- W581102801 modified "2023-09-24" @default.
- W581102801 title "Konvülziyon ve karpopedal spazm ile acil servise başvuran tip 1 otoimmün poliglandüler sendrom ve heliotropik raş birlikteliği" @default.
- W581102801 doi "https://doi.org/10.16948/zktb.48477" @default.
- W581102801 hasPublicationYear "2008" @default.
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