Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Pediatric Nephrology

Volumn 24, Issue 12, 2009, Pages 2369-2373

  Frishberg, Yaacov ^a   Dinour, Dganit ^b   Belostotsky, Ruth ^a   Becker Cohen, Rachel ^a   Rinat, Choni ^a   Feinstein, Sofia ^a   Navon Elkan, Paulina ^a   Ben Shalom, Efrat ^a  

^a HEBREW UNIVERSITY   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

Children; CLCN5 mutations; Dent's; Focal glomerulosclerosis; Nephrotic proteinuria

Indexed keywords

GENE PRODUCT; PROTEIN CLCN5; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHILD; DENT DISEASE; FOCAL GLOMERULOSCLEROSIS; HUMAN; KIDNEY TUBULE DISORDER; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEINURIA; X CHROMOSOME LINKED DISORDER;

BIOPSY; CALCIUM; CHILD; CHILD, PRESCHOOL; CHLORIDE CHANNELS; CODON, NONSENSE; CREATININE; DNA; DNA MUTATIONAL ANALYSIS; GENETIC DISEASES, X-LINKED; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; KIDNEY; MALE; METABOLIC CLEARANCE RATE; PROTEINURIA;

EID: 70350624692     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-009-1299-2     Document Type: Article

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