• Can this test be performed at home?

Yes, home sample collection is available for this test through our platform for the convenience of the patient.

• What does a positive mutation result mean?

It indicates the patient likely requires a specific vitamin-based treatment plan under medical supervision to prevent neurological decline.

SLC19A3 Genetic Test Price in Saudi Arabia

Lahalak Medical PlatformDifferentiate Care

SLC19A3 Genetic Test Price in Saudi Arabia | Lahalak Medical Platform

Medical notice: this information is for education and service understanding. It is not a diagnosis or a recommendation for an unnecessary procedure.

About this service

Accurate genetic screening of the SLC19A3 gene to detect mutations causing Basal Ganglia Disease, facilitating vitamin-based treatment plans to mitigate neurological symptoms and prevent brain damage.

Importance of Early Testing

Enables precise diagnosis of encephalopathy types that respond to vitamin therapy.
Prevents permanent neurological disabilities by initiating biotin and thiamine treatment early.
Provides clear answers for families with unexplained neurological symptoms.

Target Groups

Children experiencing sudden onset seizures or muscle weakness.
Patients with MRI findings showing changes in the basal ganglia.
Families with a known genetic history of SLC19A3-related disorders.

What the Analysis Evaluates

The test identifies pathogenic mutations in the SLC19A3 gene.
Determines if the condition is the biotin-thiamine responsive type.
Assists clinicians in tailoring vitamin dosages based on the genetic profile.

What is included?

✓Blood or saliva sample collection
✓SLC19A3 gene sequencing
✓Detailed genetic report

Conditions and notices

Fasting is not required
Previous medical reports preferred
No prior fasting required

Frequently Asked Questions

Short answers to the FAQs published with this service.

• What is the SLC19A3 gene test?

It is a genetic test that identifies mutations in a specific gene causing a basal ganglia disease treatable with high doses of biotin and thiamine.

• Does the test require fasting?

No, fasting is not required for this genetic analysis; it can be performed at any time of the day.

• How is the sample collected?

A simple blood sample is drawn from a vein, or in some cases, a buccal (cheek) swab may be used.

• How long does it take to get results?

Due to the complexity of genetic sequencing, results typically take between 2 to 4 weeks.

Service resources and references

References and additional resources

Reference material and files associated with this service when available.

Scientific references

National Center for Biotechnology Information (NCBI)
Saudi Society of Medical Genetics

Screen for Genetic Brain Health

About this service

Importance of Early Testing

Target Groups

What the Analysis Evaluates

What is included?

Conditions and notices

Frequently Asked Questions

References and additional resources

Scientific references

Choose a provider and branch

Let us help you

Didn’t find the service?

Services you might also like

Precise MALT Lymphoma Genetic Screening

Phosphatase Proteins Level Test

Genetic Test for Alpha-1 Antitrypsin

Precise Alagille Syndrome Diagnosis

Your opinion matters

Was this content helpful?

Have a note?