Literature DB >> 9198040

Von Hippel-Lindau disease: an important differential diagnosis of polycystic kidney disease.

G Browne1, J A Jefferson, G D Wright, A E Hughes, C C Doherty, N C Nevin, J A Keogh.   

Abstract

Von Hippel Lindau disease is a dominantly inherited familial cancer syndrome, characterized by retinal, spinal, and cerebellar haemangioblastomas, renal cell carcinomas, and phaeochromocytomas. Cysts of the kidney and pancreas may also occur. We describe a large three-generation Irish family with VHL disease who initially presented with features typical of autosomal dominant polycystic kidney disease. Eight clinically affected individuals were found. Visceral complications were particularly prominent within the family. There were no cases of retinal angiomata or phaeochromocytoma. The diagnosis was confirmed by genetic linkage analysis in this family, although the exact mutation has yet to be defined.

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Year:  1997        PMID: 9198040     DOI: 10.1093/ndt/12.6.1132

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  2 in total

Review 1.  Renal involvement in tuberous sclerosis complex and von Hippel-Lindau disease: shared disease mechanisms?

Authors:  Brian J Siroky; Maria F Czyzyk-Krzeska; John J Bissler
Journal:  Nat Clin Pract Nephrol       Date:  2009-03

2.  Loss of vhl in the zebrafish pronephros recapitulates early stages of human clear cell renal cell carcinoma.

Authors:  Haley R Noonan; Ana M Metelo; Caramai N Kamei; Randall T Peterson; Iain A Drummond; Othon Iliopoulos
Journal:  Dis Model Mech       Date:  2016-08-01       Impact factor: 5.758

  2 in total

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