CADASIL Genetic Health Risk Testing

NT $2,500
ABOUT US $83.3

   

CADASIL Genetic Health Risk Testing

CADASIL Genetic Health Risk Testing

Testing time10 days
Testing methodSwab
1

Website purchase, ship to the house

2

Self-screening, safe and secure

3

Superstore refrigerated, return mail insight

Product introduction

Taiwan-specific stroke mutation gene
 
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common hereditary cerebral arteriole lesion caused by a single gene mutation, NOTCH3 gene. According to the survey, 230,000 people in Taiwan have NOTCH3 gene mutations and may even have cerebrovascular disease without knowing it. Mutations in the NOTCH3 gene cause inherited intermolecular lesions in the brain, ultimately affecting brain function.
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