Polyglandular Autoimmune Syndrome Type I - StatPearls - NCBI Bookshelf
2023年3月20日 · Autoimmune polyglandular syndrome type 1 (APS-1), also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), is characterized by the triad of hypoparathyroidism, Addison disease, and chronic mucocutaneous candidiasis.
Autoimmune Polyglandular Syndrome Type 1 - Symptoms, …
2018年6月26日 · Autoimmune polyglandular syndrome type 1 (APS-1) is a rare and complex recessively inherited disorder of immune-cell dysfunction with multiple autoimmunities. It presents as a group of symptoms including potentially life-threatening endocrine gland and …
Polyglandular syndromes type I, II, III - Autoimmune Association
Autoimmune polyglandular syndrome type 1 is an inherited autoimmune condition that affects many of the body’s organs. Symptoms often begin in childhood or adolescence and may include mucocutaneous candidiasis, hypoparathyroidism, and Addison disease.
Autoimmune Polyglandular Syndromes - Endotext - NCBI Bookshelf
2024年7月21日 · autoimmune polyglandular syndrome 1 (aps1-apeced) APS1 is characterized by 3 classical features; muco-cutaneous candidiasis, hypoparathyroidism with hypocalcemia, hyperphosphatemia, and low PTH concentrations, as well as Addison disease with cortisol deficiency, occasional aldosterone deficiency, and marked elevations in adrenocorticotropic ...
APS Type 1 Foundation | Autoimmune Polyglandular Syndrome Type 1
The APS Type 1 Foundation unites and empowers a global community to drive awareness, education, and groundbreaking research for APS Type 1, transforming lives affected by this rare autoimmune disorder.
APECED & APS-1 | Immune Deficiency Foundation - Primary Immune
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), also known as autoimmune polyglandular syndrome type-1 (APS-1) or polyglandular autoimmune (PGA) syndrome type-1, is a primary immunodeficiency disease caused by variants in the autoimmune regulator (AIRE) gene.
APS-1 (APECED) - National Institute of Allergy and Infectious Diseases ...
Autoimmune polyglandular syndrome type 1 (APS-1), also called autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), is a genetic immune disorder. This disorder has a diverse range of symptoms, including autoimmunity against different organs and an increased susceptibility to candidiasis, a fungal infection caused by Candida ...
Autoimmune polyglandular syndrome type 1 - DermNet
Autoimmune polyglandular syndrome type 1 (APS1) is an autoimmune condition that results in insufficiencies of multiple endocrine glands. It is also known as autoimmune polyendocrine syndrome type 1, polyendocrinopathy-candidiasis– ectodermal dystrophy (APECED), Whitaker syndrome, and candidiasis-hypoparathyroidism–Addison disease syndrome ...
Polyglandular Autoimmune Syndrome Type I - PubMed
Autoimmune polyglandular syndrome type 1 (APS-1) is also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). It is an autoimmune disease which is characterized by a triad of hypoparathyroidism, Addison disease, and chronic mucocutaneous candidiasis.
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), also known as autoimmune polyglandular syndrome type-1 (APS-1), is a rare monogenic autoimmune disease caused by loss-of-function mutations in the autoimmune regulator (AIRE) gene.
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