Autoimmune Polyglandular Syndrome Type 1
What's New
Last Posted: Mar 04, 2023
- Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA.
Wang Yabing, et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 0 (12) 2254-2263 - Monocytic Cytokines in Autoimmune Polyglandular Syndrome Type 2 Are Modulated by Vitamin D and HLA-DQ.
Kraus Anna U, et al. Frontiers in immunology 2020 0 583709 - Severe weight loss in a hypothyroid patient as an acute presentation of autoimmune polyglandular syndrome type II.
Silajdzija Elvira, et al. Hormones (Athens, Greece) 2022 0 (2) 317-322 - Autoimmune Regulator Gene Polymorphisms in Egyptian Systemic Lupus Erythematosus Patients: Preliminary Results.
Attia Doaa Hs, et al. International journal of rheumatology 2021 0 5546639 - Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
Tomer Yaron, et al. Journal of autoimmunity 2015 6 32-9 - HLA-DQB1 Position 57 Defines Susceptibility to Isolated and Polyglandular Autoimmunity in Adults: Interaction With Gender.
Kraus Anna U, et al. The Journal of clinical endocrinology and metabolism 2019 6 (6) 1907-1916 - Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant.
Grubic Zorana, et al. Gene 2018 6 - A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
Pazderska Agnieszka, et al. The Journal of clinical endocrinology and metabolism 2016 9 jc20162368 - Association Studies of the GPR103 and BCL2L15 Genes in Autoimmune Thyroid Disease in the Japanese Population.
Ban Yoshiyuki, et al. Frontiers in endocrinology 2016 0 92 - Association of TNF-a, CTLA4, and PTPN22 polymorphisms with type 1 diabetes and other autoimmune diseases in Brazil.
Tavares N A C, et al. Genetics and molecular research : GMR 2015 0 (4) 18936-44 - Meta-analysis of STAT4 and IFIH1 polymorphisms in type 1 diabetes mellitus patients with autoimmune polyglandular syndrome type III.
de Azevêdo Silva J, et al. Genetics and molecular research : GMR 2015 0 (4) 17730-8 - Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism.
Lambert Anne-Sophie, et al. The Journal of clinical endocrinology and metabolism 2014 3 (3) E469-73 - Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III.
Addobbati C J C, et al. Genetics and molecular research : GMR 2015 0 (1) 29-33 - Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients.
Fourati Hajer, et al. Human immunology 2012 7 (7) 740-6 - Clinical and genetic characteristics of autoimmune polyglandular syndrome type 3 variant in the Japanese population.
Horie Ichiro, et al. The Journal of clinical endocrinology and metabolism 2012 6 (6) E1043-50 - Autoimmune polyglandular syndrome type 2 shows the same HLA class II pattern as type 1 diabetes.
Weinstock C, et al. Tissue antigens 2011 4 (4) 317-24 - Autoimmune polyglandular syndrome type 1
From NCATS Genetic and Rare Diseases Information Center - Autoimmune polyglandular syndrome type 2
From NCATS Genetic and Rare Diseases Information Center - Autoimmune polyglandular syndrome type 3
From NCATS Genetic and Rare Diseases Information Center - Shared molecular amino acid signature in the HLA-DR peptide binding pocket predisposes to both autoimmune diabetes and thyroiditis.
Menconi Francesca, et al. Proceedings of the National Academy of Sciences of the United States of America 2010 9 (39) 16899-903 - Autoimmune thyroiditis and diabetes: dissecting the joint genetic susceptibility in a large cohort of multiplex families.
Villano Maria Justina B, et al. The Journal of clinical endocrinology and metabolism 2009 4 (4) 1458-66 - Susceptibility alleles and haplotypes of human leukocyte antigen DRB1, DQA1, and DQB1 in autoimmune polyglandular syndrome type III in Japanese population.
Hashimoto Kozo, et al. Hormone research 2005 0 (5) 253-60 - HLA-DQA1*0301-associated susceptibility for autoimmune polyglandular syndrome type II and III.
Wallaschofski H, et al. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2003 2 (2) 120-4
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
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