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Molecular Characterization of a Cohort of 73 Patients With Infantile Spasms Syndrome
Infantile Spasms syndrome (ISs) is a characterized by epileptic spasms occurring in clusters with an onset in the first year of life. West syndrome represents a subset of ISs that associates spasms in clusters, a hypsarrhythmia EEG pattern and a developmental arrest or regression. Aetiology of ISs is widely heterogeneous including many genetic causes. Many patients, however, remain without etiological diagnosis, which is critical for prognostic purpose and genetic counselling. In the present study, the investigators performed genetic screening of 73 patients with different types of ISs by array-CGH and molecular analysis of 5 genes: CDKL5, STXBP1, KCNQ2, and GRIN2A, whose mutations cause different types of epileptic encephalopathies, including ISs, as well as MAGI2, which was suggested to be related to a subset of ISs.
Age
0 - 15 years
Sex
ALL
Healthy Volunteers
No
Start Date
October 1, 2010
Primary Completion Date
July 1, 2012
Completion Date
July 1, 2012
Last Updated
August 31, 2016
41
ACTUAL participants
Lead Sponsor
Hospices Civils de Lyon
NCT06315829
NCT03976076
NCT00441896
Data Source & Attribution
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