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Nephrology Dialysis Transplantation, Vol 14, Issue 4 936-940, Copyright © 1999 by Oxford University Press

BRIEF REPORTS

Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney disease

H Neumann, B Krumme, V van Velthoven, M Orszagh and K Zerres
Department of Nephrology, Department of Neurosurgery, Department of Neuroradiology, Albert-Ludwigs-University Freiburg, Freiburg, Germany; Department of Human Genetics, Friedrich-Wilhelms-Universitat Bonn, Bonn, Germany; Corresponding author address: Medizinische Universitatsklinik, Hugstetter Strasse 55, D-79106 Freiburg, Germany

Autosomal recessive polycystic kidney disease (ARPKD) is usually characterized by early onset chronic renal failure due to innumerable dilated collecting ducts. Hepatic fibrosis is an obligate sign. Here, for the first time, we report a 31-year-old female with ARPKD who was diagnosed with symptomatic multiple intracranial aneurysms, a manifestation previously only known to be associated with autosomal dominant polycystic kidney disease (ADPKD). Keywords: autosomal recessive polycystic kidney disease; multiple intracranial aneurysms
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