SYMPOSIUM “DRAVET SYNDROME AND OTHER SODIUM CHANNEL RELATED ENCEPHALOPATHIES”

Internacionalni simpozij "Dravet syndrome and other sodium channel related encephalopathies" održan je 15.-17.03.2018. u Veroni u organizaciji Dravet Italia Onlus i Dravet Syndrome European Federation  pod vodstvom najvećih svjetskih stručnjaka. Oni su prezentirali najnovija saznanja iz područja molekularne genetike, životinjskih modela, primjene novih lijekova, povezanosti genetike i kognitivnih ishoda kod pacijenata, istraživanja smrtnosti i mogućih uzroka.

Sudjelovanje na konferenciji omogućila je hrvatskim stručnjacima dodatnu edukaciju o Dravet sindromu i drugim rezistentnim epileptičkim sindromima s krajnjim ciljem prilagođavanja tretmana pacijenta za bolji zdravstveni ishod.

Program simpozija:

Renzo Guerrini: From Dravet syndrome to sodium channel encephalopathies

Jeffrey Noebels: Sodium channel and human disease

Ingrid E. Scheffer: SCN1A related phenotypes

Rima Nabbout: Beyond the epilepsies in SCN1A diseases

Massimo Mantegazza: Mechanisms and models of SCN1A mutations

Vania Broccoli: SCN1A epigenome editing by the CRISPR/Cas9 system restores excitability and firing activity in Dravet inhibitory interneurons

Helen Cross: Cannabinoids in the treatment of Dravet syndrome

Renzo Guerrini: Stiripentol

Lieven Lagae: Fenfluramine in Dravet syndrome: Results of a phase 3 randomized, double-blind, placebo-controlled trial

Federico Vigevano: Management of prolonged seizure from prehospital treatment to intensive care unit

Francesca Darra: Long-term outcome of Dravet syndrome

Domenica Battaglia: Teenagers-Clinical cases

Francesca Ragona: Adults-Clinical cases

Pierre Genton: Long-term outcome of patients with Dravet syndrome: the Marseille experience

Bernardo Dalla Bernardina i Charlotte Dravet: a 40 year retrospective view of Dravet syndrome

Carla Marini: Dravet syndrome and its mimics

Markus Wolff: Phenotypic spectrum of SCN2A related disorders, treatment options and outcome

Andreas Brunklaus: The genetics of SCN2A

Holger Lerche: Mechanisms and models-SCN2A

Rikke Steensbjerre Moller: The genetics of SCN8A ena Gardella: Phenotypic spectrum of SCN8A-related disorders and treatment option outcome

Miriam H. Meisler: SCN8A mutations-mechanisms and models

 

Malo doživljaja sa simpozija možete pogledati :

http://www.horizonsdravet.eu/gallery-events/

Zahvaljujemo Zračnoj luci Split i Čistoći Split d.o.o. koji su nam potpomogli da ostvarimo svoj cilj.