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Autoimmune polyendocrine syndrome type 1

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Living with Autoimmune Polyendocrine Syndrome Type 1

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Autoimmune Polyendocrinopathy Syndrome Type 1 Mnemonic

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APS Type 1

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APS Type 1 Foundation Using NORD & NIH to Advance Research

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Schmidt's disease (Autoimmune Polyendocrinopathy Type 2) Mnemonic

Autoimmune polyendocrine syndrome type 1 (APS-1), also known as autoimmune polyendocrinopathy-candidiasis–ectodermal dystrophy/dysplasia (APECED), autoimmune polyglandular syndrome type 1, Whitaker syndrome, or candidiasis-hypoparathyroidism–Addison's disease syndrome, is a subtype of autoimmune polyendocrine syndrome in which multiple endocrine glands dysfunction as a result of autoimmunity. It is a genetic disorder inherited in autosomal recessive fashion due to a defect in the AIRE gene , which is located on chromosome 21 and normally confers immune tolerance.
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  • Signs and symptoms 

  • Genetics 

  • Diagnosis 

  • Treatment