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MECP2 for RETT syndrome (Exon 2, 3 and 4)

฿15,390.00

Additional information

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
Product tags: Developmental Delays, Family History of Genetic Disorders, Genetic Disorders, Loss of Motor Skills, Rett Syndrome, Rett Syndrome Genetic Testing
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

Description

Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.

Additional information

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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