C3 glomerulonephritis associated with complement factor B mutation

American Journal of Kidney Diseases

Volumn 65, Issue 3, 2015, Pages 520-521

  Sethi, Sanjeev ^a   Smith, Richard J H ^b   Dillon, John J ^a   Fervenza, Fernando C ^a  

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; ALTERNATIVE COMPLEMENT PATHWAY C3 C5 CONVERTASE; BENAZEPRIL; COMPLEMENTARY DNA; CORTICOSTEROID; CREATININE; GLUTAMIC ACID; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; COMPLEMENT COMPONENT C3;

ADULT; C3 GLOMERULONEPHRITIS; CASE REPORT; CORTICOSTEROID THERAPY; CREATININE BLOOD LEVEL; CREATININE CLEARANCE; DISEASE EXACERBATION; ELECTRON MICROSCOPY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GLOMERULONEPHRITIS; HEMATURIA; HUMAN; HUMAN TISSUE; IMMUNOFLUORESCENCE TEST; INFECTION; KIDNEY BIOPSY; KIDNEY FUNCTION; LETTER; MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS; PROTEIN URINE LEVEL; PROTEINURIA; RENAL REPLACEMENT THERAPY; TREATMENT RESPONSE; YOUNG ADULT; GENETICS; MUTATION;

COMPLEMENT C3; COMPLEMENT FACTOR B; FEMALE; GLOMERULONEPHRITIS; HUMANS; MUTATION; YOUNG ADULT;

EID: 84924197711     PISSN: 02726386     EISSN: 15236838     Source Type: Journal    
DOI: 10.1053/j.ajkd.2014.10.023     Document Type: Letter

References (4)

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2. S. Sethi, F.C. Fervenza, and Y. Zhang C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up Kidney Int 82 2012 465 473
3. E. Goicoechea de Jorge, C. Harris, and J. Esparza-Gordillo Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome Proc Natl Acad Sci U S A 104 2007 240 245
4. Marinozzi MC, Vergoz L, Rybkine T, et al. Complement factor B mutations in atypical hemolytic uremic syndrome - disease-relevant or benign? [published online ahead of print March 20, 2014]. J Am Soc Nephrol. http://dx.doi.org/10.1681/ASN.2013070796.