Nephrotic-range Albuminuria as the presenting symptom of Dent-2 disease

Italian Journal of Pediatrics

Volumn 41, Issue 1, 2015, Pages

  De Mutiis, Chiara ^a   Pasini, Andrea ^a   La Scola, Claudio ^a   Pugliese, Fabrizio ^a   Montini, Giovanni ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

CLCN5; Dent disease; Hypercalciuria; Low molecular weight proteinuria (LMWP); OCRL; p.Arg318Cys

Indexed keywords

ALPHA 1 MICROGLOBULIN; BETA 2 MICROGLOBULIN;

ALBUMINURIA; ARTICLE; CASE REPORT; CHILD; DENT 2 DISEASE; DENT DISEASE; GENE; GENE MUTATION; HUMAN; HUMAN TISSUE; KIDNEY BIOPSY; MALE; MINIMAL CHANGE GLOMERULONEPHRITIS; MISSENSE MUTATION; MUTATIONAL ANALYSIS; OCRL GENE; PHENOTYPIC VARIATION; PROTEINURIA; SCHOOL CHILD; SYMPTOM ASSESSMENT; BIOPSY; COMPLICATION; DIFFERENTIAL DIAGNOSIS; FOLLOW UP; GENETIC DISEASES, X-LINKED; GLOMERULUS FILTRATION RATE; METABOLISM; NEPHROLITHIASIS; URINE;

ALBUMINURIA; BIOPSY; CHILD; DIAGNOSIS, DIFFERENTIAL; FOLLOW-UP STUDIES; GENETIC DISEASES, X-LINKED; GLOMERULAR FILTRATION RATE; HUMANS; MALE; NEPHROLITHIASIS;

EID: 84933512105     PISSN: 17208424     EISSN: 18247288     Source Type: Journal    
DOI: 10.1186/s13052-015-0152-4     Document Type: Article

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