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               <dc:title>Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome : Insights from the ENVISION natural history study</dc:title>
               <dc:creator>Perry, M.S.</dc:creator>
               <dc:creator>Scheffer, I.E.</dc:creator>
               <dc:creator>Sullivan, J.</dc:creator>
               <dc:creator>Brunklaus, A.</dc:creator>
               <dc:creator>Boronat, Susana</dc:creator>
               <dc:creator>Wheless, J.W.</dc:creator>
               <dc:creator>Laux, L.</dc:creator>
               <dc:creator>Patel, A.D.</dc:creator>
               <dc:creator>Roberts, C.M.</dc:creator>
               <dc:creator>Dlugos, D.</dc:creator>
               <dc:creator>Holder, D.</dc:creator>
               <dc:creator>Knupp, K.G.</dc:creator>
               <dc:creator>Lallas, M.</dc:creator>
               <dc:creator>Phillips, S.</dc:creator>
               <dc:creator>Segal, E.</dc:creator>
               <dc:creator>Smeyers, P.</dc:creator>
               <dc:creator>Lal, D.</dc:creator>
               <dc:creator>Wirrell, E.</dc:creator>
               <dc:creator>Zuberi, Sameer M</dc:creator>
               <dc:creator>Brünger, T.</dc:creator>
               <dc:creator>Wojnaroski, M.</dc:creator>
               <dc:creator>Maru, B.</dc:creator>
               <dc:creator>O'Donnell, P.</dc:creator>
               <dc:creator>Morton, M.</dc:creator>
               <dc:creator>James, Emma S.</dc:creator>
               <dc:creator>Vila, M.C.</dc:creator>
               <dc:creator>Huang, N.</dc:creator>
               <dc:creator>Gofshteyn, J.S.</dc:creator>
               <dc:creator>Rico, S.</dc:creator>
               <dc:creator>Universitat Autònoma de Barcelona</dc:creator>
               <dc:subject>Dravet syndrome</dc:subject>
               <dc:subject>ENVISION</dc:subject>
               <dc:subject>Communication/language delays</dc:subject>
               <dc:subject>Developmental and epileptic encephalopathy</dc:subject>
               <dc:subject>Natural history study</dc:subject>
               <dc:description>Dravet syndrome (DS) is a developmental and epileptic encephalopathy characterized by high seizure burden, treatment-resistant epilepsy, and developmental stagnation. Family members rate communication deficits among the most impactful disease manifestations. We evaluated seizure burden and language/communication development in children with DS. ENVISION was a prospective, observational study evaluating children with DS associated with SCN1A pathogenic variants (SCN1A+ DS) enrolled at age ≤5 years. Seizure burden and antiseizure medications were assessed every 3 months and communication and language every 6 months with the Bayley Scales of Infant and Toddler Development 3rd edition and the parent-reported Vineland Adaptive Behavior Scales 3rd edition. We report data from the first year of observation, including analyses stratified by age at Baseline: 0:6-2:0 years:months (Y:M; youngest), 2:1-3:6 Y:M (middle), and 3:7-5:0 Y:M (oldest). Between December 2020 and March 2023, 58 children with DS enrolled at 16 sites internationally. Median follow-up was 17.5 months (range =.0-24.0), with 54 of 58 (93.1%) followed for at least 6 months and 51 of 58 (87.9%) for 12 months. Monthly countable seizure frequency (MCSF) increased with age (median [minimum-maximum] = 1.0 in the youngest [1.0-70.0] and middle [1.0-242.0] age groups and 4.5 [.0-2647.0] in the oldest age group), and remained high, despite use of currently approved antiseizure medications. Language/communication delays were observed early, and developmental stagnation occurred after age 2 years with both instruments. In predictive modeling, chronologic age was the only significant covariate of seizure frequency (effect size =.52, p =.024). MCSF, number of antiseizure medications, age at first seizure, and convulsive status epilepticus were not predictors of language/communication raw scores. In infants and young children with SCN1A+ DS, language/communication delay and stagnation were independent of seizure burden. Our findings emphasize that the optimal therapeutic window to prevent language/communication delay is before 3 years of age.</dc:description>
               <dc:date>2024</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>Epilepsia ; Vol. 65 Núm. 2 (february 2024), p. 322-337</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
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