Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting 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.
MECP2 for RETT syndrome (Exon 2, 3 and 4)
Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.
15,390 THB
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Diseases : Genetic Disorders, Rett Syndrome
Symptoms : Developmental Delays, Loss of Motor Skills
Habits : Family History of Genetic Disorders
Age Groups : Adolescents, Pediatric
Specimens : EDTA Whole Blood
Diagnostic Methods : PCR and Direct Sequencing
| Also Known As | Rett Syndrome Genetic Testing |
|---|---|
| Specimen | EDTA whole blood >= 3 mL |
| Turnaround Time | 1 month |
| Test Code | MD-NLM002 |
| Test Type | Special |
| Related Tests | Genetic Testing for Neurodevelopmental Disorders |
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