DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 48 · April 2017 DOI: 10.1055/s-007-33900


Abstracts of the 43rd Annual Meeting of the Society for Neuropediatrics
Bad Nauheim, 27. to 30.04.2017

Chair: Prof. Dr. Bernd A. Neubauer, MD, Department of Pediatric Neurology, University Hospital Giessen, Giessen, Germany
Abstracts (HTML) List of Authors
P01
Mohr, N.; Schneider, J.; Spors, B.; Aliatakis, N.; John, R.; Seidel, U.; Kaindl, A.: Radiological Changes in Patients with Spina Bifida
P02
Werner, C.; Luo, X.; Elfring, G.; Kroger, H.; Riebling, P.; Ong, T.; Spiegel, R.; Peltz, S. W.: Meta-analyses of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
P03
Werner, C.; Kroger, H.; Luo, X.; McIntosh, J.; Trifillis, P.; Rodriguez, J.; Ong, T.; Riebling, P.; Souza, M.; Spiegel, R.; Peltz, S. W.: Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial
P04
Domscheit, S.; Holterhus, P.; Stephani, U.: Type 1 Diabetes and Epilepsy in Children: Is There a Pathogenetic Association between Frequency, Manifestation, and Antibodies?
P05
Adler, C.; Hessenauer, M.; Lipp, J.; Kunze, S.; Geigenberger, C.; Hörning, A.; Schaudeck, M.; Berweck, S.; Staudt, M.: Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP
P06
Preis, F.; Esser, G.; Wyschkon, A.: Innovation on the BUEVA-III: Basic Diagnostics of Developmental Disorders in Preschool Age—Version III
P07
Vieker, S.; Pfaffenberger, B.; Fischer, I.; Schmitt, J.; Rupprecht, T.: Drug-Resistant Focal Epilepsy in Infancy with the Development of a West Syndrome in DEPDC5 Mutation: Can Genetic Results Open up Therapeutic Pathways?
P09
Lüsebrink, N.; Schmitz, N.; Schubert-Bast, S.; Kieslich, M.: MEF2C Mutations: The Cause of an Epileptic Encephalopathy Syndrome with Pathognomonic Fidgetiness and Myoclonias
P10
Christ, S.; Leypoldt, F.; Hanebeck, B.; Haber, B.; Brösse, I.; Schmitt, C.; Hoffmann, G.; Syrbe, S.; Ziegler, A.: Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody
P11
Schoene-Bake, J.-C.; Hethey, S.; Wilker, M.; Weidemann, J.; Kruse, B.; Prawitz; Weiner, V.; Christen, H.-J.: Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis
P12
Coci, E. G.; Auhuber, A.; Langenbach, A.; Mrasek, K.; Riedel, J.; Leenen, A.; Lücke, T.; Liehr, T.: Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy
P13
Duckwitz, H.; Weise, S.: Pharmacological Treatment of Stimulus-Induced Drop Episodes in Children with Coffin-Lowry Syndrome: Case Experience and an Overview of the Literature
P14
Schwerin-Nagel, A.; Haber, E.; Brunner-Krainz, M.; Gruber-Sedlmayr, U.; Boltshauser, E.: 4H Leukodystrophy: A Rare Movement Disorder
P15
Drenckhahn, A.; Klaassen, S.; Varon-Mateeva, R.; Stenzel, W.; Kaindl, A.: Dilatative Cardiomyopathy and Severe Cardiac Dysfunction in a Patient with CCFDN Syndrome
P16
Brösse, I.; Assmann, B.; Reunert, J.; Ries, M.; Kölker, S.; Hoffmann, G. F.; Marquardt, T.; Syrbe, S.: Niemann-Pick Type C Disease: A Challenge in Diagnostics, Therapy, and Care for Affected Families
P17
Kauffmann, B.; Günther, L.; Jundt, G.; Junker, K.; Witt, O.; Pekrun, A.: Everolimus as a Therapy of a Benign, Infiltrative Growing Bone Tumor of the Mandibula: A Rare Manifestation with Tuberous Sclerosis
P18
Illsinger, S.; Dabke, P.; Chao, M. M.; Kratz, C.; Stange, M.; Gburek-Augustat, J.; Hartmann, H.; Das, A.: Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive
P19
Brackmann, F.; Türk, M.; Gratzki, N.; Rompel, O.; Jungbluth, H.; Schröder, R.; Trollmann, R.: Compound Heterozygous RYR1 Mutation in a Preterm with Arthrogryposis and Core Myopathy with Prenatal CNS Bleedings
P20
Decker, C.; Köhler, C.; Thiels, Ch.; Lücke, T.: Unexpected Cause of Progressive Decrease in Sensorimotor Function of the Left Leg
P21
Tountopoulou, M.; Roggenkamp, V.; Weschke, B.; Kaindl, A. M.: Lacosamide Lowers Valproate and Levetiracetam Levels
P22
Stange, M.; Illsinger, S.; Gburek-Augustat, J.; Hartmann, H.: Hyperkinetic Movement Disorder as First Manifestation of an Autoimmune Disease
P23
Zellner, H.; Baumann, M.; Albrecht, U.; Sigl, Baumgartner S.; Gedik, A.; Zeiner, F.; Baumgartner, J.; Winkler, S.; Zotter, S.; Egger, S.; Heinz-Erian, E.; Kößler, M.; Lechner, C.; Zschocke, A.; Haberlandt, E.: Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck
P24
Mörsdorf, L.; Costard, S.; Neumann, H.; Lücke, T.: Difficulties in the Acquisition of Literacy in Children with Rolandic Epilepsy or Rolandic EEG Pattern
P25
Neu, A.; Stockebrand, M.; Isbrandt, D.; Choe, C. U.: Distinct Regulation of Orexigenic and Anorexigenic Hypothalamic Pathways in Creatine-Deficient Mice
P26
Anastasopoulos, C.; Reisert, M.; Kellner, E.: “Nora Imaging”: A Web-Based Platform for Medical Imaging
P27
Hentschel, F.; Wittmack, E.; Sarpong-Bengelsdorf, A.; Roggenkamp, V.; Funk, J.; Wolter, S.; Tafelski, S.; Schulz, M.; van Riesen, A.: Rehabilitative Outcome after Selective Dorsal Rhizotomy (SDR)
P28
Pechmann, A.; Langer, T.; Schorling, D.; Eckenweiler, M.; Wider, S.; Kirschner, J.: Single-Center Experience with Intrathecal Administration of Nusinersen in Children with Spinal Muscular Atrophy Type I
P29
Karenfort, M.; Molle, Krause Z.; Müller, K.; Beez, T.: GAD65-Positive Limbic Encephalitis and Large Temporal Arachnoid Cyst: A Diagnostic Conundrum
P30
Weber, C.; Weber, H.; von der Hagen, M.; Schallner, J.: Assessment of Anthropometric Measures and Hand Muscle Strength in Children to Establish Standardized Parameters for Pediatric Neurorehabilitation
P31
Keil, A.; Kölbel, H.; Sanchez, I.; Kress, W.; Schara, U.: Case Report: Gamma-Sarcoglycanopathy Plus RYR1- and TCAP-Mutations: Do Further Mutations Explain Clinical Variations in Phenotypes of Neuromuscular Diseases?
P32
Fiedler, B.; Althaus, J.; Schwartz, O.; Niederstadt, T.; Schilling, M.; Kurlemann, G.: Unilateral Atrophy of the Tongue: Hypoglossal Palsy Due to Neurovascular Contact?
P33
Jelesch, E.; König, H.; Weir, S.; Weinberger, R.; Herzig, N.; Kluger, G.; Michel, J.; Bernius, P.; von Kries, R.; Narayanan, U.; Schröder, S.; Berweck, S.: GOAL: Gait Outcome Assessment List
P34
Goerlach, J.; Hahn, A.; Heidenreich, Y.; Vanlander, A.; Van Coster, R.; Schänzer, A.: The Impact of Morphometric Skin Punch Biopsy Analysis for a Small Nerve Fiber Involvement in Children with Pain Syndrome
P35
Thiels, Ch.; Yoon, M.-S.; Rostásy, K.; Köhler, C.; Lücke, T.: Plasmapheresis as at Treatment Option in Anti-MOG–Related Neurological Disorders with Fulminant Progress
P36
Henzi, B.; Bartholdi, D.; Wildbolz, M.; Kohler, B.; Bürki, S.; Perret, E.; Strozzi, S.; Schindler, K.; Gallati, S.; Bigi, S.: Northern Epilepsy: Not So Northern Anymore
P37
Bulst, S.; Nissen, A. M.; Rapp, C.; Graf, J.; Mayer, V.; Benet-Pagès, A.; Reilich, P.; Walter, M. C.; Holinski-Feder, E.; Abicht, A.: CNV Detection from Targeted Next-Generation Panel Sequencing Data Increases the Diagnostic Yield in Patients with Neuromuscular Diseases
P38
Fischer, M.; Hanff, E.; Kayacelebi, A. A.; Pross, S.; Siefen, R.; Emons, B.; Tsikas, D.; Lücke, T.: The L-Arginine/NO Pathway in Children with Attention-Deficit/Hyperactivity Disorder (ADHD)
P39
Otten, K.; Bauder, F.; Kröll, J.; Röthlisberger, B.; Schmitt-Mechelke, Th.: Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins
P40
Mayer, V.; Bulst, S.; Reilich, P.; Walter, M. C.; Abicht, A.: Titinopathies in Human Genetics Diagnostics
P41
Plesko-Altermatt, N.; Grunt, S.; Diepold, M.; Perret-Hoigné, E.; Horvath, T.; Steinlin, M.; Bigi, S.: Transient Ischemic Attack (TIA): A Problem Not to Miss
P42
Bley, A.; Löbel, U.; Denecke, J.: Compassionate Use of Simvastatin for a Patient with Juvenile Metachromatic Leukodystrophy
P43
Aliatakis, N.; Schneider, J.; Lebek, S.; Seidel, U.; Kaindl, A. M.: Pathological Fractures in Patients with Myelomeningocele
P44
Dillenberger, S.; Klein, M.; Schwindt, W.; Kasprzak, B.; Althaus, J.; Fiedler, B.; Kurlemann, G.: Midaortic Syndrome in TSC
P45
Spenner, B.; Krois-Neudenberger, J.; Kurlemann, G.; Althaus, J.; Schwartz, O.; Schmidt, R.; Fiedler, B.: Are Reemergence of Sleep Spindles and Cessation of Hypsarrhythmia Prognostic Factors for Neurodevelopmental Outcome in Adults with a History of West Syndrome in Infancy?
P46
Tüngler, V.; König, N.; Engel, K.; Smitka, M.; Ungerath, K.; von der Hagen, M.; Berner, R.; Lee-Kirsch, M. A.: Effects of Janus Kinase Inhibition in Two Children with Aicardi-Goutières Syndrome
P47
Althaus, J.; Kurlemann, G.; Fiedler, B.; Schwartz, O.; Niederstadt, T.; Sträter, R.: Forceful Monitoring after Acute Pediatric Stroke Can Help Identify the Etiology
P48
Rügner, S.; Naumann, N.; Lorenz, I.; Rompel, O.; Trollmann, R.: Toxic Rapidly Progressive Myelopathy Induced by Nelarabine in an Adolescent with Relapsed Pre-T-ALL
P49
Pschibul, A.; Gierthmühlen, M.; Müller-Felber, W.; Korinthenberg, R.: Progressive Radial Motor Neuropathy Due to a Perineurioma in an Adolescent Girl: Case Report
P50
Kappl, S.; Haßlberger, T.; Sturm, E.; Bangert, H.; Nader, S.; Berweck, S.: Development of a Classification System for Wheelchair Maintenance and Seat Positioning
P51
Kappl, S.; Lange, J.; Herberhold, T.; Berweck, S.: A Technical Neuro-Orthopedic and Neuropediatric Report on Requirements Needed for a Successful Rehabilitation of a Disabled Adolescent
P52
Kuhnke, N.; Younossi, M.; Paul, D.; Klotz, D.; Wusthoff, C.; Jacobs-Le Van, J.: High-Frequency Oscillations in Surface EEG Recorded from Neonates with Perinatally Acquired Hypoxic Ischemic Encephalopathy: A Retrospective Study
P53
Weiss, D.; Denecke, J.; Johannsen, J.: Respiratory Distress and Encephalopathy: Fat Embolism Syndrome in Duchenne Muscular Dystrophy
P54
Moontaha, S.; von Spiczak, S.; Scharlach, S.; Doege, C.; Boor, R.; May, T.; Stephani, U.; Siniatchkin, M.; Galka, A.: Evaluation of the Effects of Anticonvulsive Therapy in Children with Symptomatic Epilepsy by a State Space Modeling Approach
P55
von Spiczak, S.; Klein, K.-M.; Kluger, G. J.; Lemke, J. R.; Neubauer, B. A.; Weber, Y. G.: Recommendations for Diagnostic Genetic Testing in Epilepsies
P56
Schwartz, O.; Althaus, J.; Fiedler, B.; Heß, K.; Paulus, W.; Hörtnagel, K.; Biskup, S.; Kurlemann, G.: Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation
P57
Schrank, W.; Lampe, C.; Knuf, M.: Two Siblings with D-Bifunctional Protein Deficiency and Unusual Clinical Course
P58
Karabul, N.; Marquardt, T.; Petersen, M.; Beckmann, A.; Namal, E.; Lücke, T.: Globotriaosylsphingosine (Lyso-GB3 bzw. Lyso-GL3), an Excellent Biomarker for Children with Fabry Disease
P59
Lippert, L.; Wicht, S.; Lampe, Ch.; Wiemer-Kruel, A.; Knuf, M.: Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”
P60
Wunderlich, S.; Lampe, C.; Tan, I.; Knuf, M.: Health-Related Quality of Life in Children and Adolescents with Spinal Dysraphic Disorders
P61
Stapper, T.; Valcheva, D.; Höll, T.; Rosenbaum, T.: Everolimus Reduces Seizure Frequency in Tuberous Sclerosis Complex
P62
Dursun, N.; Tilton, A.; Gormley, M.; Bonikowski, M.; Velez, J. C.; Rodriguez, M. L.; Picaut, P.; Grandoulier, A. S.; Delgado, M. R.: Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity
P63
Delgado, M. R.; Tilton, A.; Carranza, J.; Bonikowski, M.; Dursun, N.; Catus, F.; Picaut, P.: Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design
P64
Osinski, D.; Leis, Th.; Abicht, A.; Trollmann, R.: BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report