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Lahalak Medical PlatformDifferentiate Care
NOTCH3 Gene Molecular Analysis (CADASIL)
Identify genetic risks for hereditary stroke and vascular dementia using advanced NOTCH3 gene analysis, enabling early clinical diagnosis and informed family health planning for patients.
A molecular analysis detecting mutations in the NOTCH3 gene associated with CADASIL syndrome. It accurately evaluates risks for recurrent strokes and hereditary vascular dementia for patients.
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