| Literature DB >> 25403779 |
Anna Hogendorf1, Beata S Lipska-Zietkiewicz2, Agnieszka Szadkowska1, Maciej Borowiec1,3, Magdalena Koczkowska2, Piotr Trzonkowski4, Izabela Drozdz1, Krystyna Wyka1, Janusz Limon2, Wojciech Mlynarski1.
Abstract
A girl with 18q deletion syndrome was diagnosed with autoimmune diabetes mellitus and Hashimoto's thyroiditis at the age of 3 yr. In addition, the girl suffered from recurrent infections due to immunoglobulin A and IgG4 deficiency. She was also found to have CD3+CD4+FoxP3+, CD3+CD4+FoxP3+CD25+, and CD3+CD4+CD25+CD127 regulatory T cells deficiency. The exceptional coincidence of the two autoimmune disorders occurring at an early age, and associated with immune deficiency, implies that genes located on deleted 19.4 Mbp region at 18q21.32-q23 (chr18:58,660,699-78,012,870) might play a role in the pathogenesis of autoimmunity leading to β cell destruction and diabetes.Entities:
Keywords: 18q deletion syndrome; Hashimoto's thyroiditis; IgA deficiency; diabetes mellitus
Mesh:
Year: 2014 PMID: 25403779 DOI: 10.1111/pedi.12235
Source DB: PubMed Journal: Pediatr Diabetes ISSN: 1399-543X Impact factor: 4.866