POSTER SESSION 2: Epilepsy: Diagnosis and Investigations
Tracks
POSTER AREA
| Wednesday, September 18, 2019 |
| 12:15 PM - 1:00 PM |
| POSTER AREA (Balcony Muses Foyer) |
Overview
P02-01 to P02-52
Speaker
Dr. Zvonka Rener Primec
Ljubljana University Medical Centre & Medical Faculty, University Ljubljana
P02-01 | Refractory infantile spasms in a boy with Down Syndrome and Koolen-De Vries Syndrome
Prof. Faruk Incecik
Cukurova Universitesi Tip Fakultesi
P02-02 | Co-existence of Type 1 Diabetes Mellitus and Periventricular Heterotopia in a child: a case report
Prof. Pelagia Vorgia
University Of Crete
P02-03 | Whole Exome Sequencing (WES) limitations in diagnosis of early Infantile Encephalopathy
Dr. Aalt van Roest
University Hospital Antwerp Belgium
P02-04 | The clinical difference between infants with PRRT2-Positive and infants with PRRT2-Negative Cluster Epilepsy
Dr. Alfons Macaya
Vall d'Hebron University Hospital
P02-05 | Muscarinic Acetylcholine receptor M1 mutation causing early Infantile Epileptic Encephalopathy
Dr. Andreea Nissenkorn
Sheba Medical Center
P02-06 | Mutation in the KCNQ2 ion selectivity filter causing severe Epileptic Encephalopathy responsive to Retigabine
Dr. An-Sofie Schoonjans
Antwerp University Hospital
P02-07 | Therapeutic drug monitoring of Fenfluramine and its metabolite Norfenfluramine in patients with Dravet Syndrome
Dr. Antonio Hedrera Fernández
Hospital Universitario Central de Asturias
P02-08 | Reflex Hot Water Epilepsy in children: Spanish multicentre retrospective study
Dr. Birendra Rai
Northampton General Hospital, UK
P02-09 | ALG13 de novo pathogenic mutation in a male child with Congenital Heart Disease and vertebral abnormalities
Dr. Bülent Kara
Kocaeli University Medical Faculty
P02-10 | Diagnostic rate of targeted gene panel analysis of patients with early-infantile Epileptic Encephalopathy
Dr. Bülent Kara
Kocaeli University Medical Faculty
P02-11 | Alternative approaches to conventional antiepileptic drugs in early infantile Epileptic Encephalopathies: Galactose and Inositol therapies for SLC35A2 and PLCB1 gene mutations
Dr. Elena Maqueda Castellote
Hospital Universitari Parc Tauli
P02-12 | Neonatal Epilepsy and genetic testing: a new approach
Dr. Emanuela Izzo
Biomarin.
P02-13 | Utility of gene panel testing in children with seizure onset after 2 years of age: results from a European and Middle Eastern Epilepsy genetic testing programme
Ms. Evelina Iachim
Pediatric Neurology Department, Doctor Victor Gomoiu Children's Hospital, Bucharest, Romania
P02-14 | Infantile spasms without Hypsarrhythmia – A distinct Epileptic Syndrome? – A series of 5 patients
Ms. Evelina Iachim
Pediatric Neurology Department, Doctor Victor Gomoiu Children's Hospital, Bucharest, Romania
P02-15 | A case at the crossroads of Neurology and Cardiology
Dr. Gorande Kanabar
East & North Herts Nhs Trust
P02-16 | Reflex seizures in “Benign Myoclonic Epilepsy in Infancy”
Dr. Jelena Radic Nisevic
KBC RIJEKA
P02-17 | Chromosome microarray in children with Epilepsy and neurological abnormalities – Our experience
Dr. Kristina Lotha
Leeds Teaching Hospital Nhs Trust
P02-18 | SLC6A1 variant in a child with Intractable Epilepsy
Dr. Leanid Shalkevich
Belarusian Medical Academy of Post-graduate Education
P02-19 | The risks of Epilepsy after the first attack in children
Dr. Madina Taghiyeva
Azerbaijan Medical University
P02-20 | Cerebral Palsy and Epilepsy
Mrs. Maria Papadopoulou
Child Neurology Unit, 4th Pediatric Department, Aristotle University Of Thessaloniki, 'Papageorgiou Hospital'
P02-21 | Evaluation of the cognitive side effects of antiepileptic treatment in children and adolescents with Epilepsy by the Test Epitrack® Junior
Dr. Monika Kukuruzovic
UHC Sestre milosrdnice
P02-22 | Infantile spasms – How often do we think of vitamin B12 deficiency
Dr. Munni Ray
Leeds Teaching Hospitals NHS Trust
P02-23 | Successful Epilepsy surgery outcome in a child with Mesial Temporal Sclerosis whose initial EEGs were suggestive of benign Focal Epilepsy
Dr. Elif Naz Kadem
Antalya Research and Training Hospital
P02-24 | CLN5 mutation causing Neuronal Ceroid Lipofuscinosis: a case report
Dr. Neslihan Bilgin
Hacettepe University
P02-25 | Clinical and neuroimaging findings in patients with benign Focal Epileptiform Discharges of childhood
Dr. Deniz Yuksel
Sami Ulus Çocuk Hastanesi
P02-26 | Paediatric Status Epilepticus: a retrospective overview
Dr. Paola De Liso
Bambino Gesù Children's Hospital, Irccs
P02-27 | Fatal Status Epilepticus in Dravet Syndrome: an acute Encephalopathy triggered by fever
Mrs. Pinar Arican
Kahramanmaraş Necip Fazıl Hospital
P02-28 | Bisphenol A levels in children with acute seizures
Mrs. Pinar Arican
Kahramanmaraş Necip Fazıl Hospital
P02-29 | A new cause of electrical Status Epilepticus in sleep: CDKL5 Disorder
Dr. Piyatida Jongruk
Chiang Mai University
P02-30 | Risk factors of Epilepsy in children with complex febrile seizures; a retrospective cohort study
Dr. Prerna Choudhury
Noah's Ark Childrens' Hospital, Cardiff Uk
P02-31 | The aetiology of Epilepsia Partialis Continua: a cautionary tale
Dr. Shoaib Khan
Royal Aberdeen Children Hospital
P02-32 | Jeavons Syndrome: challenges in diagnosis and treatment
Dr. Silvia Masnada
University Of Pavia
P02-33 | Aicardi Syndrome: clinical and neuroradiological phenotype associations
Dr. Stella Mouskou
Children's Hospital "P & Aglaia Kyriakou"
P02-34 | A novel DEPDC5 mutation and a known pathogenic mutation in CLCN1 gene in a family with Epilepsy and a variable phenotype
Dr. Tetiana Stetsenko
Shupik national medical academy of postgraduate education
P02-35 | Case of Focal Frontal Epilepsy in a 3 months-child with mutation of the NRPL3 gene
Mrs. Tetyana Yanina
Children Republic Clinical Hospital
P02-36 | Electroencephalographic changes in children with Autism Spectrum Disorders
Dr. Thomas Foiadelli
IRCCS Policlinico San Matteo Foundation
P02-37 | Use of SISCOM for the identification of the epileptogenic zone in children
Dr. Inyang Takon
Queen Elizabeth II Hospital, East And North Hertfordshire Nhs Trust
P02-38 | Psychogenic Non-epileptic Seizures (PNES): a retrospective study on outcomes in a general hospital paediatric service in the United Kingdom
Dr. Ye-Hwa Jun
The Catholic University of Korea, Seoul, Korea, Republic of
P02-39 | Changes in background electroencephalographic activity in benign childhood Epilepsy with centrotemporal spikes after Oxcarbazepine treatment: a Standardized Low-Resolution Brain Electromagnetic Tomography (sLORETA) study
Ms. Joana Chiara Mecca
Centro Universitário Estácio De Ribeirão Preto
P02-40 | DHX30 gene mutations: a new cause of Neurodevelopmental Disorder associated with refractory seizures
Ms. Luciana do Prado Rocha
Centro Universitário Estácio de Ribeirão Preto
P02-41 | Expanding the clinical phenotype of DEAF1-Associated Neurodevelopmental Disorder (DAND) gene mutations: two new cases displaying different neurological presentations
Mr. Sergey Burd
N. I. Pirogov Russian National Research Medical University, Ministry Of Health Of Russia, Moscow
P02-42 | Problems of sustainability of rendering medical assistance to patients sufficiating Epileption during transition them from the children's network to adult practice
Mr. Tony Yu
University Of Edinburgh Medical School
P02-43 | Investigating structural brain abnormalities on Neuroimaging in Paediatric Epilepsy
Dr. Maria Spanou
Attikon University Hospital
P02-44 | Spinal Muscular Atrophy and Progressive Myoclonic Epilepsy. Report of a Greek paediatric patient
Mrs. Melpomeni Giorgi
"Attiko" University Hospital, National and Kapodistrian University of Athens
P02-45 | Heterogeneity in early Infantile Epileptic Encephalopathies other than SCN1A – Description of 21 cases
Dr. Sofia Quintas
Hsm-chln
P02-46 | Genetic Epileptic Encephalopathies: review and analysis of diagnostic paradigm from a tertiary centre
Mrs. Tatjana Kovacevic-Preradovic
Sachsonian Epilepsy Centre Kleinwachau
P02-47 | Soccer and seizures – Case report of teenagers with exercise-induced Epilepsy
Mrs. Anna Baró Serrano
Hospital Infantil Vall Hebron
P02-48 | A Severe phenotype of early Infantile Epileptic Encephalopathy associated with mutation in CPLX1
Ms. Hikaru Kitahara
Department Of Pediatrics, Osaka Medical College, Osaka, Japan
P02-49 | 17 cases of late onset spasms
Ms. Lucía Dougherty De Miguel
Hospital Vall D’hebron (barcelona)
P02-50 | Neonatal onset Epileptic Encephalopathy, a new CACNA1C-related phenotype
Prof. Dilsad Turkdogan
Marmara University, Medical Faculty, Department Of Pediatric Neurology
P02-51 | Diagnostic yield of WES following aCGH in the genetic aetiology of early onset Epileptic Encephalopathies
Dr. Roberto Santalucia
Erasme University Hospital - Free University Of Brussels
P02-52 | SLC13A5-related Encephalopathy with Epilepsy in the neonatal period: remarkable improvement on Carbamazepine and Pyridoxal-Phosphate. What worked out so well?
Chair
Dana Craiu
“Carol Davila” University of Medicine, Bucharest, Romania
Pinelopi Dragoumi
Aristotle University Of Thessaloniki
