← Back to catalog
Genetic Testing
Genetic Diagnosis of Friedreich's Ataxia (FXN)
4 900 som
Turnaround: 7–14 business days
Blood draw — 80 som (included in packages)
Description
A genetic test for mutations linked to Friedreich's ataxia (FXN 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 Kennedy's Disease (AR)4 900 som
- Genetic Diagnosis of Charcot-Marie-Tooth Disease Type 1A (PMP22)4 900 som
- Genetic Diagnosis of Myotonic Dystrophy Type 1 (DMPK)4 900 som
- Genetic Diagnosis of Myotonic Dystrophy Type 2 (CNBP)4 900 som
- Genetic Diagnosis of Primary Dystonia Type 1 (DYT1)4 800 som
- Sports Genetics: Individual Traits for Selecting an Effective and Safe Training Regimen, with Geneticist's Report4 800 som
