Phenotypic Heterogeneity in Pediatric Autosomal Dominant Polycystic Kidney Disease at First Presentation: A Single-Center, 20-Year Review

American Journal of Kidney Diseases

Volumn 43, Issue 2, 2004, Pages 296-303

  Tee, James B ^a,b   Acott, Philip D ^a   Heather McLellan, D ^a   Crocker, John F S ^a  

^a DALHOUSIE UNIVERSITY   (Canada)

^b IWK HEALTH CENTRE   (Canada)

Author keywords

Autosomal dominant polycystic kidney disease (ADPKD); Pediatric; Polycystic kidney disease (PKD); Presentation; Risk factors

Indexed keywords

CREATININE;

ADOLESCENT; ADULT; CLINICAL FEATURE; COMORBIDITY; CREATININE CLEARANCE; DISEASE COURSE; ECHOGRAPHY; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; FOLLOW UP; HUMAN; HYPERLIPIDEMIA; HYPERTENSION; KIDNEY FUNCTION; KIDNEY POLYCYSTIC DISEASE; LIVER CYST; MAJOR CLINICAL STUDY; PANCREAS CYST; PHENOTYPE; PROTEINURIA; REVIEW; SCHOOL CHILD; SPLEEN CYST;

EID: 0742305472     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.ajkd.2003.10.017     Document Type: Article

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