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

被引：27

作者：

Neumann, HPH

Krumme, B

van Velthoven, V

Orszagh, M

Zerres, K

机构：

[1] Univ Freiburg, Med Klin, Dept Nephrol, D-79106 Freiburg, Germany

[2] Univ Freiburg, Dept Neurosurg, D-79106 Freiburg, Germany

[3] Univ Freiburg, Dept Neuroradiol, D-79106 Freiburg, Germany

[4] Univ Bonn, Dept Human Genet, D-5300 Bonn, Germany

来源：

NEPHROLOGY DIALYSIS TRANSPLANTATION | 1999年 / 14卷 / 04期

关键词：

autosomal recessive polycystic kidney disease; multiple intracranial aneurysms;

D O I：

10.1093/ndt/14.4.936

中图分类号：

R3 [基础医学]; R4 [临床医学];

学科分类号：

1001 ; 1002 ; 100602 ;

摘要：

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 lime, 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).

引用

页码：936 / 939

页数：4

共 19 条

[1] TRAUMATIC CEREBRAL ANEURYSMS - CLINICAL FEATURES AND NATURAL-HISTORY [J].