← Back to catalog
Genetic Testing
Genetic Diagnosis of Fragile X-Associated Tremor/Ataxia Syndrome (FMR1)
5 800 som
Turnaround: 7–14 business days
Blood draw — 80 som (included in packages)
Description
A genetic test for mutations linked to fragile X-associated tremor/ataxia syndrome (FMR1 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.
Not sure which test you need?
Ask a question on WhatsAppSimilar tests
- Genetic Diagnosis of Spinocerebellar Ataxias (SCA1, 2, 3, 6, 7; Friedreich's Ataxia)5 800 som
- Genetic Diagnosis of Hereditary Forms of Parkinson's Disease6 100 som
- Thrombophilia Predisposition Genes - Extended Panel5 500 som
- Genetic Diagnosis of Huntington's Disease (HTT)5 300 som
- Hereditary Predisposition to Type 2 Diabetes5 300 som
- EGFR T790M Mutation Detection (blood)6 590 som