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Lahalak Medical PlatformDifferentiate Care
Brown-Vialetto-Van Laere Syndrome Gene Sequencing (SLC52A2/SLC52A3)
An advanced genetic test to detect mutations in SLC52A2 and SLC52A3 genes, aiding in the accurate diagnosis of the rare Brown-Vialetto-Van Laere syndrome for better clinical management.
This test involves full gene sequencing to identify genetic changes associated with Brown-Vialetto-Van Laere syndrome. It confirms clinical diagnosis and helps assess hereditary risks for affected families.
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