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Article

Clinico-pathologic findings in medullary cystic kidney disease type 2.

Pediatric nephrology (Berlin, Germany) - 1 Jun 2005

Bleyer Anthony J, Hart Thomas C, Willingham Mark C, Iskandar Samy S, Gorry Michael C, Trachtman Howard

Abstract excerpt

Medullary cystic kidney disease type 2 is an uncommon autosomal dominant condition characterized by juvenile onset hyperuricemia, precocious gout and chronic renal failure progressing to end-stage renal disease in the 4th through 7th decades of life. A family suffering from this condition is described. The patient in the index case presented with renal insufficiency as a child. A renal biopsy revealed tubular...

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PMID: 15844001
DOI: 10.1007/s00467-004-1719-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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