A Case Report of IPEX Syndrome with Neonatal Diabetes Mellitus and Congenital Hypothyroidism as the Initial Presentation, and a Systematic Review of neonatal IPEX
Author:
Funder
Key R&D Guidance Plan Projects in Liaoning Province
Shengjing Hospital
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
https://link.springer.com/content/pdf/10.1007/s10875-023-01456-0.pdf
Reference60 articles.
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2. Martin F, et al. Human FOXP3 and cancer. Oncogene. 2010;29(29):4121–9.
3. Bennett CL, et al. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat Genet. 2001;27(1):20–1.
4. d’Hennezel E, et al. The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome. J Med Genet. 2012;49(5):291–302.
5. Martin-Santiago A, et al. Diagnostic value of the skin lesions in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. Pediatr Dermatol. 2013;30(6):e221–2.
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1. IPEX syndrome from diagnosis to cure, learning along the way;Journal of Allergy and Clinical Immunology;2023-11
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