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SCN8A epilepsy

Infantile epileptic encephalopathy 13 (EIEE13)
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Overview

Type of Disease: Genetic, autosomal dominant Pediatric onset Intellectual disability (no physical disability) Rare Condition or Disease

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Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

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The Cute Syndrome Website
Added On: Jun 11, 2019
Category: General
SCN8A Epilepsy is a rare disorder and it is still in the early stages of being diagnosed and understood. Our team at The Cute Syndrome Foundation is working hard to bring SCN8A into the light, to fund researchers and help families.