Endocrine Abstracts

Introduction: Autoimmune polyglandular syndrome type 1 (APS-1) is a rare autosomal recessive disorder characterized by autoimmune multiorgan attack. Clinical manifestations are widely variable. Treatment is based on supplementation of the various deficiencies and the prognosis is variable.Case: An 18-year-old female presented with nail dystrophy and candida infection at age 7. Then, she was diagnosed with primary hyporparathyroidism and Addison’s di...