Dent's disease

Nephrology Dialysis Transplantation

Volumn 20, Issue 10, 2005, Pages 2284-2285

  Neild, Guy H ^a   Thakker, Rajesh V ^b   Unwin, Robert J ^a   Wrong, Oliver M ^a  

^a MIDDLESEX HOSPITAL   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

CLCN5 gene; Dent's disease; Nephrocalcinosis; Renal cysts

Indexed keywords

CLCN5 PROTEIN; DNA; GENE PRODUCT; UNCLASSIFIED DRUG;

ADULT; BLOOD ANALYSIS; CASE REPORT; DENT DISEASE; DNA SEQUENCE; FAMILIAL DISEASE; GENE DELETION; GLUCOSURIA; HEMODIALYSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; KIDNEY CALCIFICATION; KIDNEY COLIC; KIDNEY CYST; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; MALE; MUTATIONAL ANALYSIS; NEPHROLITHIASIS; NOTE; PRIORITY JOURNAL; PROTEINURIA; RENOGRAPHY; URETER STONE; X CHROMOSOME;

ADULT; CHLORIDE CHANNELS; CHROMOSOMES, HUMAN, X; GENETIC DISEASES, X-LINKED; HUMANS; MALE; NEPHROCALCINOSIS; POLYCYSTIC KIDNEY DISEASES;

EID: 27144525029     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfh968     Document Type: Note

References (4)

1. Lloyd SE, Pearce SHS. Fisher SE et al. A common molecular basis for three inherited kidney stone diseases. Nature, 1996; 379: 445-449
2. +-ATPase without ultrastructural change in kidneys of Dent's disease patients. Kidney Internat 2003; 63: 1285-1295
3. Wrong OM, Norden AGW, Feest TG. Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. Q J Med, 1994; 87: 473-493
4. Wrong, O. Nephrocalcinosis. In: Davidson AM. Cameron JS. Grünfeld J-P et al. (eds), Oxford University of Textbook of Clinical Nephrology. 3rd edn. Oxford University Press. 2005, pp. 1257-1279