Journal Article

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

H P Neumann, B Krumme, V van Velthoven, M Orszagh and K Zerres

in Nephrology Dialysis Transplantation

Published on behalf of European Renal Association - European Dialysis and Transplant Assoc

Volume 14, issue 4, pages 936-939
Published in print April 1999 | ISSN: 0931-0509
Published online April 1999 | e-ISSN: 1460-2385 | DOI: http://dx.doi.org/10.1093/ndt/14.4.936
Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney disease.

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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).

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Subjects: Nephrology

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