Nutcracker syndrome: a potentially underdiagnosed cause of proteinuria in children with familial Mediterranean fever
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology, and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-021-05337-9.pdf
Reference24 articles.
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3. Chae JJ, Cho YH, Lee GS, Cheng J et al (2011) Gain-of-function pyrin mutations induce NLRP3 protein-independent interleukin-1β Activation and severe autoinflammation in mice. Immunity 34:755–768. https://doi.org/10.1016/j.immuni.2011.02.020
4. Goldfinger SE (1972) Colchicine for Familial Mediterranean Fever. N Engl J Med 287:1302. https://doi.org/10.1056/NEJM197212212872514
5. Özkaya N, Yalçinkaya F (2003) Colchicine treatment in children with familial Mediterranean fever. Clin Rheumatol 22:314–317. https://doi.org/10.1007/s10067-003-0739-9
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1. Nutcracker syndrome in pediatrics: initial findings and long-term follow-up results;Pediatric Nephrology;2023-09-21
2. Diagnostic Clues in Pediatric Nutcracker Syndrome: From Two Clinical Cases to Current Literature Analysis;Children;2022-12-17
3. Erysipelas-Like Erythema: A Manifestation of Severe Disease Phenotype in Pediatric Patients with Familial Mediterranean Fever;Turkish Archives of Pediatrics;2022-10-25
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