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Neurol India ; 2004 Mar; 52(1): 99-101
Article in English | IMSEAR | ID: sea-121361

ABSTRACT

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an inherited arterial disease, commonly overlooked or misdiagnosed. We report a case of CADASIL in a 51 years old woman who presented with progressive subcortical dementia, recurrent ischemic events and seizures in the absence of known vascular risk factors of five years' duration. Her mother had a history of similar illness. Magnetic resonance imaging (MRI) of brain revealed subcortical and deep white matter hyperintense lesions within the cerebral white matter on T2-weighted images. DNA mutation of Notch 3 gene confirmed the diagnosis of CADASIL.


Subject(s)
Brain/pathology , CADASIL/genetics , Fatal Outcome , Female , Humans , India , Magnetic Resonance Imaging , Middle Aged , Neurologic Examination
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