Graves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome

Author:

Ueda Yoko1,Uraki Shinsuke1,Inaba Hidefumi1,Nakashima Sakiko1,Ariyasu Hiroyuki1,Iwakura Hiroshi1,Ota Takayuki1,Furuta Hiroto1,Nishi Masahiro1,Akamizu Takashi1

Affiliation:

1. The First Department of Medicine, Wakayama Medical University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

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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