Glomerulocystic kidney disease

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Glomerulocystic kidney disease in a family.

BACKGROUND Glomerulocystic kidney disease (GCKD) is a rare renal disorder, the identity of which has long been discussed. GCKD can occur in a familial form with autosomal dominant transmission. The presence of GCKD in families affected with autosomal dominant polycystic kidney disease (ADPKD) has lent support to the hypothesis that GCKD may be an early manifestation of ADPKD. In families with h...

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Glomerulocystic disease

Glomerulocystic disease is a rare cause of cystic kidney diseases and can occur at any age. It is characterized by cystic dilatation of the Bowman's capsule and normal tubules, and needs to be differentiated from other cystic renal diseases. It commonly presents as renal failure. We present a case of a 52-year-old female, with renal failure who was subsequently found to have glomerulocystic dis...

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Selective Dicer Suppression in the Kidney Alters GSK3β/β-Catenin Pathways Promoting a Glomerulocystic Disease

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Glomerulocystic Kidney Disease and Hepatoblastoma in an Infant: A Rare Presentation

Glomerulocystic kidney disease (GCKD) is a rare condition comprising heritable and non-heritable types [Oh et al.: Nephron 1986;43:299-302]. Hepatoblastoma is a sporadically occurring tumor of embryonal origin that is associated with overgrowth syndrome and renal cysts. A concurrent presentation of GCKD with hepatoblastoma was first described in 1989 [Rao et al.: Jpn J Surg 1989;19:583-585]. We...

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Glomerulocystic kidney disease in an adult presenting as end-stage renal failure.

Key words: adult glomerulocystic kidney disease; end-cell counts and platelets were normal, as were prothrombin and partial thromboplastin times. Serum stage renal failure; renal biopsy concentrations of albumin and gamma globulins were normal. Total haemolytic complement, C 3 and C 4 were within normal range and the Wassermann reaction was

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ژورنال

عنوان ژورنال: Pediatric Nephrology

سال: 2010

ISSN: 0931-041X,1432-198X

DOI: 10.1007/s00467-009-1416-2