Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation

Pediatric Nephrology

Volumn 26, Issue 3, 2011, Pages 419-424

  Leroy, Valérie ^a,c   Fremeaux Bacchi, Véronique ^b   Peuchmaur, Michel ^a   Baudouin, Véronique ^a   Deschênes, Georges ^a   MacHer, Marie Alice ^a   Loirat, Chantal ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^c HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

C3 nephritic factor; Complement alternative pathway; Dense deposit disease; Factor H; Factor I; Membranoproliferative glomerulonephritis type I

Indexed keywords

COMPLEMENT FACTOR H; FIBRINOGEN; METHYLPREDNISOLONE; NEPHRITIC FACTOR; PREDNISONE; RITUXIMAB; STEROID;

ADOLESCENT; ANKLE EDEMA; ARTICLE; CASE REPORT; CHILD; CORTICOSTEROID THERAPY; DENSE DEPOSIT DISEASE; DRUG DOSE REDUCTION; DRUG PULSE THERAPY; GENE MUTATION; GENETIC COMPLEMENTATION; GENETIC DISORDER; GENETIC REGULATION; GENETIC SCREENING; GLOMERULUS FILTRATION RATE; HEMATURIA; HETEROZYGOTE; HUMAN; MALE; MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS; NEPHROTIC SYNDROME; PERIORBITAL EDEMA; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEINURIA;

ADOLESCENT; BIOPSY; CHILD; CHILD, PRESCHOOL; COMPLEMENT C3 NEPHRITIC FACTOR; COMPLEMENT FACTOR H; COMPLEMENT FACTOR I; GENETIC PREDISPOSITION TO DISEASE; GLOMERULONEPHRITIS, MEMBRANOPROLIFERATIVE; HETEROZYGOTE; HUMANS; IMMUNOSUPPRESSIVE AGENTS; KIDNEY; MALE; MUTATION; PHENOTYPE; TIME FACTORS; TREATMENT OUTCOME;

EID: 79955028622     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-010-1734-4     Document Type: Article

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