Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
Autoimmune polyglandular syndrome type 1 (APS-1) is a very rare autoimmune entity, accounting for about 400 cases reported worldwide.It is characterized by the presence of at least two of three cardinal components: click here chronic mucocutaneous candidiasis (CMC), hypoparathyroidism and Addison’s disease.It typically manifests in childhood with