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Genetic Testing
Smith-Lemli-Opitz Syndrome, Detection of 13 Mutations in the DHCR7 Gene
8 700 som
Turnaround: 7–14 business days
Blood draw — 80 som (included in packages)
Description
A genetic test for mutations linked to Smith-Lemli-Opitz syndrome (DHCR7 gene). Used for diagnosis, carrier detection, and family planning.
When to Take This Test
- Suspected inherited disease
- Family planning, carrier status
- As directed by a geneticist
Preparation
- No special preparation needed
- Taken once — the result doesn't change over your lifetime
- Interpreted by a geneticist
This information is for reference only and does not replace a doctor's consultation.
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