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  4. Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
 
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Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Journal
Journal of the Neurological Sciences
Journal Volume
228
Journal Issue
2
Pages
125-128
Date Issued
2005
Author(s)
SUNG-CHUN TANG  
MING-JEN LEE  
JIANN-SHING JENG  
Yip P.-K.
DOI
10.1016/j.jns.2004.10.019
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-13444304264&doi=10.1016%2fj.jns.2004.10.019&partnerID=40&md5=a4120b97a4248933ae4690640ed18b3c
https://scholars.lib.ntu.edu.tw/handle/123456789/590579
Abstract
The phenotype and genotype of cerebral autosomal dominant arteriopathy and subcortical infarcts and leukoencephalopathy (CADASIL) in Caucasians have been well characterized, but CADASIL is less recognized in Asian populations. Here we investigated the first known Taiwanese family affected by CADASIL and identified an uncommon NOTCH3 mutation. The family had clinical manifestations in affected members including recurrent strokes, early dementia, and depression, but not migraine. A skin biopsy in the proband patient showed characteristic pathological findings of CADASIL on electron microscopy. Afterward, genetic analysis found an Arg332Cys mutation at exon 6 of NOTCH3. Neuropsychological evaluation showed vascular dementia in two of four affected people. Head MRI showed multiple infarcts in bilateral basal ganglia, thalami, periventricular white matter, external capsules, and brainstem, but involvement of the anterior temporal pole was found only in two people with milder symptoms. To our knowledge, the Arg332Cys NOTCH3 mutation at exon 6, which was identified in the studied family, has not been reported in Asian populations. Our findings emphasize the importance of genetic analysis of NOTCH3 for Asians with a phenotype typical of CADASIL. ? 2004 Elsevier B.V. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
arginine; cysteine; Notch3 receptor; adult; article; Asian; basal ganglion; brain infarction; brain stem; CADASIL; case report; clinical feature; dementia; depression; electron microscopy; exon; family study; female; gene mutation; genetic analysis; human; male; migraine; multiinfarct dementia; mutational analysis; neuropathology; neuropsychological test; nuclear magnetic resonance imaging; phenotype; priority journal; recurrent disease; skin biopsy; stroke; Taiwan; thalamus; white matter
Type
journal article

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