Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
http://link.springer.com/content/pdf/10.1007/s13730-020-00487-5.pdf
Reference14 articles.
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2. Kallel-Sellami M, Laadhar L, Zerzeri Y, Makni S. Complement deficiency and systemic lupus erythematosus: consensus and dilemma. Expert Rev Clin Immunol. 2008;4:629–37.
3. Alper CA, Xu J, Cosmopoulos K, et al. Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency. J Clin Immunol. 2003;23:297–305.
4. Kışla Ekinci RM, Balcı S, Bişgin A, Atmış B, Doğruel D, Yılmaz M. Autoimmune manifestations in heterozygote type I complement 2 deficiency: a child eventually diagnosed with systemic lupus erythematosus. Arch Rheumatol. 2019;34:96–9.
5. Spârchez M, Lupan I, Delean D, et al. Primary complement and antibody deficiencies in autoimmune rheumatologic diseases with juvenile onset: a prospective study at two centers. Pediatr Rheumatol Online J. 2015;13:51.
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