Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil?

Background C3 glomerulopathy (C3G) is a complement-mediated disease. Although genetic studies are not required for diagnosis, they are valuable for treatment planning and prognosis prediction. The aim of this study is to investigate the clinical phenotypes, kidney survival, and response to mycopheno...

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Veröffentlicht in:	Pediatric nephrology (Berlin, West) West), 2024-05, Vol.39 (5), p.1435-1446
Hauptverfasser:	Günay, Neslihan, Dursun, İsmail, Gökçe, İbrahim, Akbalık Kara, Mehtap, Tekcan, Demet, Çiçek, Neslihan, Torun Bayram, Meral, Koyun, Mustafa, Dinçel, Nida, Dursun, Hasan, Saygılı, Seha, Yürük Yıldırım, Zeynep Nagehan, Yüksel, Selçuk, Dönmez, Osman, Yel, Sibel, Demircioğlu Kılıç, Beltinge, Aydoğ, Özlem, Atmış, Bahriye, Çaltık Yılmaz, Aysun, Bakkaloğlu, Sevcan A., Aytaç, Mehmet Baha, Taşdemir, Mehmet, Kasap Demir, Belde, Soylu, Alper, Çomak, Elif, Kantar Özşahin, Aslı, Kaçar, Alper, Canpolat, Nur, Yılmaz, Alev, Girişgen, İlknur, Akkoyunlu, Kadirye Betül, Alpay, Harika, Poyrazoğlu, Hakan M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Asymptomatic Complement system Diagnosis Genotypes Kidney diseases Medical prognosis Medicine Medicine & Public Health Mutation Mycophenolate mofetil Mycophenolic acid Nephrology Original Article Patients Pediatrics Phenotypes Survival Urology
Online-Zugang:	Volltext
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