Symptomatic hypocalcemia after treatment for hyperthyroidism in a woman with chromosome 22q11.2 deletion syndrome complicated by Graves’ disease: longitudinal changes in the number of subsets of CD4 and CD8 lymphocytes after thyroidectomy
Author:
Affiliation:
1. Department of Endocrinology and Metabolism, Dokkyo Medical University, Tochigi 321-0293, Japan
2. Department of Infection Control and Clinical Laboratory Medicine, Dokkyo Medical University, Tochigi 321-0293, Japan
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/68/10/68_EJ20-0717/_pdf
Reference23 articles.
1. 1 Kobrynski LJ, Sullivan KE (2007) Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet 370: 1443–1452.
2. 2 Sullivan KE (2019) Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome. Immunol Rev 287: 186–201.
3. 3 Gennery AR, Barge D, O’Sullivan JJ, Flood TJ, Abinun M, et al. (2002) Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome. Arch Dis Child 86: 422–425.
4. 4 Ferrando-Martínez S, Lorente R, Gurbindo D, De José MI, Leal M, et al. (2014) Low thymic output, peripheral homeostasis deregulation, and hastened regulatory T cells differentiation in children with 22q11.2 deletion syndrome. J Pediatr 164: 882–889.
5. 5 Chang LS, Barroso-Sousa R, Tolaney SM, Hodi FS, Kaiser UB, et al. (2019) Endocrine toxicity of cancer immunotherapy targeting immune checkpoints. Endocr Rev 40: 17–65.
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