Congenital disorders of glycosylation: A rare cause of nephrotic syndrome

Nephrology Dialysis Transplantation

Volumn 24, Issue 8, 2009, Pages 2591-2594

  Sinha, Manish D ^a   Horsfield, Catherine ^a   Komaromy, Debbie ^a   Booth, Caroline J ^a   Champion, Michael P ^a  

^a EVELINA LONDON CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

CDG; Congenital nephrotic syndrome; Nephrotic syndrome; Proteinuria

Indexed keywords

ANTICONVULSIVE AGENT; ANTIHYPERTENSIVE AGENT; ANTITHROMBIN III; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 8; COMPLEMENT COMPONENT C1Q; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DIURETIC AGENT; GLUCOCORTICOID; IMMUNOGLOBULIN M; IMMUNOSUPPRESSIVE AGENT; PROTEIN C; PROTEIN S; TRANSFERRIN;

ANAMNESIS; ARTICLE; BLOOD TRANSFUSION; CASE REPORT; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION; DEVELOPMENTAL DISORDER; ELECTROENCEPHALOGRAM; ELECTRON MICROSCOPY; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; GLYCOSYLATION; HISTOPATHOLOGY; HUMAN; HYPERTENSION; HYPOALBUMINEMIA; INFANT; ISOELECTRIC FOCUSING; KIDNEY BIOPSY; KIDNEY HYPERTROPHY; LIVER DISEASE; MALE; MESANGIUM SCLEROSIS; MICROCEPHALY; MUSCLE HYPOTONIA; NEPHROTIC SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PROTEINURIA; SCREENING TEST; SEIZURE;

ABNORMALITIES, MULTIPLE; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; GLYCOSYLATION; HUMANS; INFANT; MALE; NEPHROTIC SYNDROME;

EID: 67651091598     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfp226     Document Type: Article

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