Objective Autoimmune polyendocrine syndrome type 1 (APS1) is a rare autosomal
recessive disorder characterized by progressive organ-specific autoimmunity. There is scant …

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) syndrome is
a rare monogenic autosomal recessive disorder caused by biallelic mutations in the AIRE …

Background Mutations of the autoimmune regulator gene (AIRE), located on chromosome
21q22. 3, are recognized as the cause of a rare monogenic organ-specific autoimmune …

Objective Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
(APECED) is a rare autosomal recessive systemic autoimmune disease caused by …

Objectives Hypoparathyroidism is a rare disease in children that occurs as a result of
autoimmune destruction of the parathyroid glands, a defect in parathyroid gland …

Background: Mutations of the autoimmune regulator gene (AIRE), located on chromosome
21q22. 3, are recognized as the cause of a rare monogenic organ-specific autoimmune …