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LOCATION B = BIEKORFZAAL + PARKING BIEKORF BELGIAN …Sep 22, 2017 · 1 Atypical anorexia as main...
Transcript of LOCATION B = BIEKORFZAAL + PARKING BIEKORF BELGIAN …Sep 22, 2017 · 1 Atypical anorexia as main...
BELGIAN SOCIETY
OF PEDIATRIC NEUROLOGY
non-profit organization
Autumn Meeting
Friday 22 September 2017
Biekorfzaal
Bruges
NEUROCUTANEOUS
DISORDERS
RNA AND DNA IN
PEDIATRIC NEUROLOGY
Registration
ONLINE REGISTRATION IS REQUIRED Please use the registration tool in the calendar section of our website www.bspn.be. Registration is only valid after payment of the registration fee. If maximum capacity is reached the online registration will be locked. PARTICIPATION FEE (ALL INCLUDED) Student: 15 € Resident: 30 € BSPN member: 50 € Non-BSPN member: 70 € No on-site registration will be accepted when the maximum capacity of the conference room is reached. PAYMENT By bank transfer to the account number IBAN: BE38 2100 0475 5072 BIC: GEBABEBB using the account name “ASBL SOCIETE BELGE DE NEUROLOGIE PEDIATRIQUE”, and mentioning “BSPN Autumn Meeting 22/9/2017” and name of the participant.
LOCATION B = BIEKORFZAAL + PARKING BIEKORF
Because of limited parking space in the city centre
we recommend the low-cost parking Centrum-Station. On showing your parking ticket at the Lijnwinkel you will receive free tickets for bus transfer to and from the centre.
General Information
ORGANIZATION: Marc D'Hooghe, AZ Sint-Jan Bruges Filip Roelens, AZ Delta Roeselare Katrien Keppens, BC Spermalie Bruges Lore Vallaeys, AZ Groeninge Kortrijk Liesbeth De Waele, UZ Leuven/AZ Groeninge LOCATION: Biekorfzaal Bruges Sint-Jakobsstraat 8 = main entrance Naaldenstraat 4 = entrance of the foyer, next to the entrance of Parking Biekorf ACCREDITATION: certificates will be provided MEETING LANGUAGE: English The short oral communications can be presented in Dutch or French with slides in English. FINAL PROGRAMME: The authors and the titles of the posters and the short oral presentations will be announced on the website of the Belgian Society of Pediatric Neurology www.bspn.be. ABSTRACTS: We invite you to submit a scientific abstract, related or unrelated to the topics of this meeting. Abstracts should be sent by email to “[email protected]” before 4 September. Please clearly indicate title, authors, address, and email address. The abstract should be typed in Word and should not exceed one A4 page. Six abstracts will be selected for oral presentation.
Programme
8:30-9:10 REGISTRATION 9:10-9:15 WELCOME SESSION I chairpersons Prof. JP. Misson - Prof. A. Jansen 9:15-9:55 Neurofibromatosis Prof. Dr. Eric Legius, Centre Human
Genetics, Univ. Hosp. Louvain 9:55-10:35 Vascular Neurocutaneous Disorders
Prof. Dr. Miika Vikkula, Human Molecular Genetics, de Duve Institute, UCL, Brussels
10:35-11:00 COFFEE & POSTERS SESSION II chairpersons Prof. G. Buyse - Prof. MC. Nassogne 11:00-11:45 Mosaic Neurocutaneous Disorders
Dr. Veronica Kinsler, Pediatric Dermatology, Great Ormond Street Hospital for Children, London, UK
11:45-12:15 Ataxia Telangiectasia and Other Recessive Ataxias based on DNA Repair Defects Prof. Dr. Michèl Willemsen, Pediatric Neurology, Radboud UMC Nijmegen, NL
12:15-12:35 Short Communications (2x) 12:35-14:10 LUNCH & POSTERS & SHORT WALK IN THE CENTRE OF BRUGES SESSION III chairpersons Prof. A. Aeby - Prof. R. Van Coster 14:10-14:50 RNA in child neurology Prof. Dr. Ir. Pieter Mestdagh, Centre
Medical Genetics, Univ. Hosp. Ghent
14:50-15:20 Gene Panels and Mendeliomes: general considerations Prof. Dr. Ir. Paul Coucke, Centre Medical Genetics, Univ. Hosp. Ghent
15:20-15:50 Genetics of Intellectual Disability Prof. Dr. Hilde Van Esch, Centre Human
Genetics, Univ. Hosp. Louvain 15:50-16:10 COFFEE & POSTERS SESSION IV chairpersons Prof. B. Ceulemans - Prof. H. Van Esch 16:10-16:50 Short Communications (4x) 16:50-17:05 Genetics of Ataxia Dr. Isabelle Vandernoot, Centre Medical
Genetics, Univ. Hosp. ULB, Brussels 17:05-17:20 Genetics of Neuromuscular Diseases Dr. Sandra Coppens and Prof. Dr. Nicolas
Deconinck, Dept. of Child Neurology, Univ. Hosp. Brugmann ULB-VUB, Brussels
17:20-17:35 Genetics of Lysosomal Storage Diseases Dr. Sc. Alexander Gheldof, Centre Medical
Genetics, Univ. Hosp. VUB, Brussels 17:35-17:50 Genetics of Cerebral Palsy
Dr. Diane Beysen and Prof. Dr. Berten Ceulemans, Dept. of Child Neurology, Univ. Hosp. Antwerp
17:50-18:00 Prof. A. Aeby, former BSPN president CONCLUSION – ANNOUNCEMENTS – AWARD FOR THE BEST RESIDENT POSTER OR SHORT ORAL COMMUNICATION 18:00-18:30 CLOSING RECEPTION
ADDITIONAL PROGRAMME BSPN MEETING 22/09/17 BRUGES
Title Author Affiliation
1 Atypical anorexia as main presenting symptom of an anti-NMDA receptor encephalitis Shari Anseeuw UZ Gent presentation
(session II 12u15)2 Electro-encephalography in childhood migraine can be useful Laurens Dobbels AZ Sint-Jan, Brugge presentation
(session II 12u25)3 Self-limited familial infantile epilepsy and PRRT2 Aalt van Roest UZA presentation
(session IV 16u10)4 Novel pathogenic variants in GLE-1 as cause of congenital, AR motorneuron disease with
extremely poor prognosis: contribution of WES
Roberto Santalucia ULB-Erasme presentation
(session IV 16u20)5 Three siblings with progressive encephalopathy and destructive white matter lesions
associated with TRAPPC9 mutations
Helen Franckx UZ Brussel presentation
(session IV 16u30)6 Inborn errors in RNA polymerase III underlie chickenpox-associated neurological
complications
Benson Ogunjimi UZA presentation
(session IV 16u40)7 PRRT2 mutation is a cause of non familial infantile focal seizure: a report of a case Despoina Mandelanaki ULB-Huderf poster
8 Initial diagnosis of cerebral palsy: à propos of two patients Dina Amrom ULB-Huderf poster
9 Idiopathic pulmonary arterial hypertension in early infancy: rule out NFU1 deficiency Stéphanie Paquay UCL poster
10 Case report: A boy with Delleman syndrome Annelien Marcelis H. Hartziekenhuis, Lier poster
11 Efficacy of sublingual lorazepam versus intrarectal diazepam for prolonged convulsions in
sub-Saharan Africa
Célestin Kaputu Kalala
Maly
CHR Citadelle - CHU
Liege
poster
12 Unusual intra-operative complication in a child with NF1 Aikaterini Monti UCL poster
13 Jaffe-Campanacci syndrome: an atypical presentation of neurofibromatosis 1 Sandrine Vaessen CHR Liège poster