Graves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome
Author:
Affiliation:
1. The First Department of Medicine, Wakayama Medical University, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/56/10/56_56.7927/_pdf
Reference25 articles.
1. 1. McDonald-McGinn DM, Sullivan KE, Marino B, et al. 22q11.2 deletion syndrome. Nat Rev Dis Primers 1: 15071, 2015.
2. 2. Burnside RD. 22q11.21 Deletion Syndromes: a review of proximal, central, and distal deletions and their associated features. Cytogenet Genome Res 146: 89-99, 2015.
3. 3. Astor MC, Løvås K, Debowska A, et al. Epidemiology and health related quality of life in hypoparathyroidism in Norway. J Clin Endocrinol Metab 101: 3045-3053, 2016.
4. 4. Gennery AR, Barge D, O'Sullivan JJ, Flood TJ, Abinun M, Cant AJ. Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome. Arch Dis Child 86: 422-425, 2002.
5. 5. Akamizu T, Mori T, Nakao K. Pathogenesis of Graves' disease: molecular analysis of anti-thyrotropin receptor antibodies. Endocr J 44: 633-646, 1997.
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