An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch
Author:
Affiliation:
1. Department of Internal Medicine, Keiaido Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/56/7/56_56.7558/_pdf
Reference64 articles.
1. 1. Bassett AS, McDonald-McGinn DM, Devriendt K, et al. Practical guidelines for managing patients with 22q11.2 deletion syndrome. J Pediatr 159: 332-339, 2011.
2. 2. McDonald-McGinn DM, Sullivan KE. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). Medicine 90: 1-18, 2011.
3. 3. Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 105: 1617-1624, 2010.
4. 4. Chow LY, Waye MM, Garcia-Barcelo M, Chiu HFK, Fung KP, Lee CY. Velo-cardio-facial syndrome, schizophrenia and deletion at chromosome 22q11. J Intellect Disabil Res 42: 184-188, 1998.
5. 5. Tastuzawa Y, Sekinaka K, Suda T, et al. An interictal schizophrenia-like psychosis in an adult patient with 22q11.2 deletion syndrome. Epilepsy Behav Case Rep 3: 36-38, 2015.
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