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Genetic Testing
Wilson's Disease, Detection of 15 Mutations in the ATP7B Gene
9 700 som
Turnaround: 7–14 business days
Blood draw — 80 som (included in packages)
Description
A genetic test for mutations linked to Wilson's disease (a disorder of copper metabolism), ATP7B gene. Used for diagnosis, carrier detection, and family planning.
When to Take This Test
- Suspected hereditary condition
- Family planning, carrier status
- As ordered by a geneticist
Preparation
- No special preparation needed
- Taken once — the result doesn't change over a lifetime
- Interpreted by a geneticist
This information is for reference only and does not replace a doctor's consultation.
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