A rare case of late-onset immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome confused with IgA vasculitis nephropathy
Author:
Funder
National Natural Science Foundation of China
Health Science and Technology Development Special Foundation of Nanjing
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00467-024-06482-7.pdf
Reference10 articles.
1. Park JH, Lee KH, Jeon B, Ochs HD, Lee JS, Gee HY, Seo S, Geum D, Piccirillo CA, Eisenhut M et al (2020) Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: a systematic review. Autoimmun Rev 19:102526. https://doi.org/10.1016/j.autrev.2020.102526
2. Barzaghi F, Amaya Hernandez LC, Neven B, Ricci S, Kucuk ZY, Bleesing JJ, Nademi Z, Slatter MA, Ulloa ER, Shcherbina A et al (2018) Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study. J Allergy Clin Immunol 141(1036–1049):e1035. https://doi.org/10.1016/j.jaci.2017.10.041
3. Halabi-Tawil M, Ruemmele FM, Fraitag S, Rieux-Laucat F, Neven B, Brousse N, De Prost Y, Fischer A, Goulet O, Bodemer C (2009) Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. Br J Dermatol 160:645–651. https://doi.org/10.1111/j.1365-2133.2008.08835.x
4. Improda N, Capalbo D, Cirillo E, Cerbone M, Esposito A, Pignata C, Salerno M (2014) Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature. BMC Pediatr 14:272. https://doi.org/10.1186/1471-2431-14-272
5. Miller P, Lei L, Charu V, Higgins J, Troxell M, Kambham N (2022) Clinicopathologic features of non-lupus membranous nephropathy in a pediatric population. Pediatr Nephrol 37:3127–3137. https://doi.org/10.1007/s00467-022-05503-7
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