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Rett Syndrome (deletions/duplication analysis on MECP2 gene)(CGC genetics)
SKU: MD-NLM665 Categories: , , , , , , , , , , , Tags: , , , , , , ,

In Stock

Rett Syndrome (deletions/duplication analysis on MECP2 gene)(CGC genetics)

฿40,000.00

Additional information

Also Known As

Rett Syndrome Gene Test, MECP2 Gene Test
Specimen

EDTA whole blood 3 ml
Turnaround Time

37 days
Test Code

MD-NLM665
Test Type

Special
Related Tests

Fragile X Syndrome, Autism Spectrum Disorder Panel

Detects deletions or duplications in the MECP2 gene, which are associated with Rett syndrome, a genetic neurological disorder that primarily affects females.

Product tags: Developmental Delays, Genetic Disorders, MECP2 Gene Test, Movement Issues, Neurological Disorders, None, Rett Syndrome Gene Test, Seizures
Diseases: Genetic Disorders, Neurological Disorders
Symptoms: Developmental Delays, Movement Issues, Seizures
Habits: None
Age Groups: Pediatrics, Women
Specimens: EDTA Whole Blood
Diagnostic Methods: Deletion/Duplication Analysis, Gene Sequencing
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Description

Detects deletions or duplications in the MECP2 gene, which are associated with Rett syndrome, a genetic neurological disorder that primarily affects females.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Rett Syndrome Gene Test, MECP2 Gene Test
Specimen

EDTA whole blood 3 ml
Turnaround Time

37 days
Test Code

MD-NLM665
Test Type

Special
Related Tests

Fragile X Syndrome, Autism Spectrum Disorder Panel

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