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Rett Syndrome (sequence and deletion/duplica- tion analysis of MECP2 gene)(CGC genetics)

฿67,200.00

Additional information

Also Known As

MECP2 Gene Test for Rett Syndrome
Specimen

EDTA whole blood 3 ml
Turnaround Time

67 days
Test Code

MD-NLM663
Test Type

Special
Related Tests

Fragile X Syndrome Test, Autism Genetic Panel
Product tags: Developmental Delays, Genetic Disorders, MECP2 Gene Test for Rett Syndrome, None, Rett Syndrome, Seizures
Diseases: Genetic Disorders, Rett Syndrome
Symptoms: Developmental Delays, Seizures
Habits: None
Age Groups: Children
Specimens: EDTA Whole Blood
Diagnostic Methods: MLPA, Sanger Sequencing

Description

Detects mutations and deletions/duplications in the MECP2 gene, which are associated with Rett syndrome, a neurodevelopmental disorder primarily affecting girls.

Additional information

Also Known As

MECP2 Gene Test for Rett Syndrome
Specimen

EDTA whole blood 3 ml
Turnaround Time

67 days
Test Code

MD-NLM663
Test Type

Special
Related Tests

Fragile X Syndrome Test, Autism Genetic Panel

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