| Literature DB >> 23774548 |
Yuki Nakada1, Ken Terui, Kazunori Kageyama, Yuko Tsushima, Hiroshi Murakami, Yasushi Soma, Takeshi Nigawara, Satoru Sakihara.
Abstract
22q11.2 Deletion syndrome is recognized to be a major cause of congenital hypoparathyroidism, and affected patients exhibit a range of autoimmune characteristics. The syndrome becomes apparent in early childhood and is rarely diagnosed in adulthood. This report describes an adult case of 22q11.2 deletion syndrome first diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis. It is important to diagnose 22q11.2 deletion syndrome in adults because such patients are still at high risk for developing treatable diseases, such as hypocalcemia and autoimmune diseases.Entities:
Mesh:
Year: 2013 PMID: 23774548 DOI: 10.2169/internalmedicine.52.9543
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271