CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.

Abstract:

:Cerebral cavernous malformations (CCM) are CNS vascular anomalies associated with seizures, headaches, and hemorrhagic strokes. The CCM1 gene was screened in 35 sporadic cases with either single or multiple CCM. It was found that 29% of the individuals with multiple CCM have a CCM1 mutation, whereas cases with only one malformation have none. Sporadic cases with multiple malformations warrant the same approach as individuals who have a familial history of CCM.

journal_name

Neurology

journal_title

Neurology

authors

Verlaan DJ,Laurent SB,Sure U,Bertalanffy H,Andermann E,Andermann F,Rouleau GA,Siegel AM

doi

10.1212/01.wnl.0000118299.55857.bb

subject

Has Abstract

pub_date

2004-04-13 00:00:00

pages

1213-5

issue

7

eissn

0028-3878

issn

1526-632X

journal_volume

62

pub_type

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