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Clinical Trial Summary

Investigators at Boston Children's Hospital are conducting research in order to better understand the genetic factors which may contribute to epilepsy and related disorders. These findings may help explain the broad spectrum of clinical characteristics and outcomes seen in people with epilepsy.


Clinical Trial Description

Many individuals with epilepsy experience seizures which respond well to treatment. Some types of epilepsy, however, are characterized by seizures which begin very early in childhood and are associated with severe intellectual and/or developmental disabilities. These conditions are often difficult to treat. The investigators' research effort is focused on identifying genetic changes (known as "DNA variants") that cause epilepsy. By doing so the investigators hope to improve diagnosis and treatment for this epilepsy. We have two specific aims: 1. Identifying genetic findings in patients with epilepsy and related disorders. 2. Correlating genetic findings with epilepsy phenotypes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01858285
Study type Observational
Source Boston Children's Hospital
Contact Beth R Sheidley, MS
Phone 8572185533
Email beth.sheidley@childrens.harvard.edu
Status Recruiting
Phase
Start date November 2010
Completion date December 2030

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