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Gene Analysis Dravet Syndrome (SCN1A)
Gene Analysis Dravet Syndrome (SCN1A) identifies mutations in the SCN1A gene, responsible for Dravet syndrome, a severe form of epilepsy that begins in infancy and leads to developmental delays and behavioral challenges.
13 days
Report Ready
No Fasting
Fasting
5-99
Age Group
Home
Collection
Preparation
Why this test
Fasting Required
Not Required
⏱ Report Time
13 days
🧫 Sample Type
Blood
🎂 Age Group
5-99
👤 Gender
Male,Female
🏠 Collection
Home Visit
Gene Analysis Dravet Syndrome (SCN1A)
Gene Analysis Dravet Syndrome (SCN1A)
