STXBP1 SYNDROME I CONFERENCE official schedule, will take place the next 3rd of November at Ágora auditorium in COSMOCAIXA , Barcelona.
9.00 to 9.25: Opening.
9.30 to 10.15: M.D. Victor Ruggieri. Head of Clinic at the Neurology Department. Pediatric Hospital “Juan P. Garrahan” from Buenos Aires, Argentina:
“Scenarios to consider facing an early infantile epileptic encephalopathy and Autism: two sides of the same coin (Applied to STXBP1 syndrome)”
10.30 to 11.15: M.D. Claudia Arberas. Head of Genetic Department. Children Hospital “Dr. Ricardo Gutiérrez” from Buenos Aires, Argentina:
“Autism and epilepsy, specific syndromes. Special consideration to STXBP1-E. Clinic, genetic and epigenetic aspects”
11:30 to 11.45: Break – Coffee.
11.45 to 12.30: M.D. Judith Armstrong Morón. Deputy doctor of the Genetic Department at Sant Joan de Déu Hospital, Barcelona (Spain):
“Approach to the genetic diagnosis in STXBP1 syndrome”.
12.45 to 13.15: Round table with the morning speakers.
13:30: Break – Lunch.
16:15 to 17:00: M.D. Alfons Macayá Ruiz. Head of Neuropediatric Department at Hospital Vall D’Hebron, Barcelona (Spain). Chairman of the Spanish Pediatric Neurology Society.
“Early infantile epileptic encephalopathy: Physiopathology and genetic”
17:15 to 18:00: M.D. Miquel Raspall Chaure. Deputy doctor of the Neuropediatric Department at Vall D’Hebron Hospital, Barcelona (Spain).
“Early infantile epileptic encephalopathy: Epidemiology, clinic and treatment”
18:00 to 18:15: Break
18:15 to 19:00: M.D. Elisenda Cortés Saladelafont. Neuropediatrician at Sant Joan de Déu hospital, Barcelona (Spain) – Neurometabolic Diseases Unit:
“Synaptic mechanisms in STXBP1”.
19:00 to 19:30: Round table with all speakers.
In order to ease the organization and logistics of this event, we request your registration for free in the link below:
Registry I STXBP1 Syndrome Conference
Limited seating, 195 seats.
Please email email@example.com for any questions related.