Molecular Genetics Dravet syndrome ( SCN1A ) gene analysis - NGS
Also Known As
SCN1A Gene Analysis, Dravet Syndrome Genetic Test, Severe Myoclonic Epilepsy of Infancy Test, Sodium Channel Gene Mutation Panel, MolGen Dravet Syndro... Read more
Test Parameters Included
SCN1A Gene Mutation Analysis - Next Generation Sequencing (NGS)Pathologist Molecular Genetics Remark - correlated with Dravet syndrome clinical featur... Read more
Department
MOLECULAR GENETICS
Methodology
NGS
Sample Required
WB EDTA
Preparation
No, fasting is not required for a molecular genetics test to analyze the SCN1A gene for Dravet syndrome diagnosis using Next Generation Sequencing (NG... Read more
Schedule Report
28 Days
Emergency Report
Yes
Frequently Asked Questions
What is Dravet syndrome?Dravet syndrome is a rare genetic epilepsy disorder characterized by intractable seizures starting in infancy, often triggered... Read more
Test Description
Test Code
MOG362
- High-end laboratory & medical equipment.
- Outstanding doctor team.
- Personalized care & high-quality service.
- Tailormade health screening packages.