DOI : 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 39 · December 2008 DOI: 10.1055/s-002-16101


Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics
Graz, 23.–26. April 2009

Chairman: Univ. Prof. Dr. Barbara Plecko, Graz
Abstracts (HTML) List of Authors
P001
Biste, M.; Madignier, F.; Freisinger, P.; Rolinski, B.; Mayr, J.; Horvarth, R.; Tesarova, M.; Sperl, W.; Meitinger, T.; Prokisch, H.: Improved molecular diagnostics for patients with respiratory chain complex deficiency
P002
Acham-Roschitz, B.; Mayr, J.; Sperl, W.; Lindbichler, F.; Bittner, R.; Mache, C. J.; Ring, E.; Plecko, B.: Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
P003
Prokisch, H.; Freisinger, P.; Abicht, A.; Kunz, W.; Wittig, I.; Obermaier-Kusser, B.; Schöls, L.; Schülke-Gerstenfeld, M.; Meitinger, T.; Klopstock, T.: mitoNET – German Network for mitochondrial disorders
P004
Klepper, J.; Ben-Omran, T.; Scheffer, H.: GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation
P005
Spiczak, S. von; Helbig, I.; Drechsel-Baeuerle, U.; Muhle, H.; van Baalen, A.; van Kempen, M. J. A.; Lindhout, D.; Stephani, U.; Keller-Stanislawski, B.: VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
P006
Hartig, M. B.; Hempel, M.; Meitinger, T.; Kmiec, T.; Prokisch, H.: Clinical characterisation of NBIA patients with and without mutation in PANK2 gene
P007
Schallner, J. C.; Hagen, M. von der; Lehmann-Horn, F.; Jurkat-Rott, K.: A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
P008
Kotzaeridou, U.; Arning, L.; Ebinger, F.; Wolf, N.: Atypical clinical presentation of a girl with episodic ataxia type II
P009
Leiz, S.; Breuer, K.; Weise, A.; Wagenstaller, J.; Daumer-Haas, C.: Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
P010
Marschik, P. B.; Oberle, A.; Vogrinec, G.; Laccone, F.; Einspieler, C.: The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
P011
Johann to Settel, E.; Siegler, N.; Fleischhack, G.: Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia
P012
Leiz, S.; Kraus, C.; Peters, J.; Daumer-Haas, C.: Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
P013
Haug, V.; Korinthenberg, R.; Omran, H.; Kirschner, J.: Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2
P014
Makowski, C.; Hempel, M.; Steinborn, M.; Burdach, S.: Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy
P015
Brocke, K. S.; Hackmann, K.; Tinschert, S.; Prokop, K.; Ikonomidou, C.; Tyshchenko, N.: Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report
P016
Panzer, A.; Deuschle, K.; Schell-Apacik, C.; Burfeind, P.; Esser, N.; Moers, A. von: CDKL5 mutation in neonatal onset of epilepsy
P017
Munk, I.; Merkel, H. J.; König, S.: Partial response to the vagus nerve stimulation in twins with double cortex syndrome
P018
Kehrer, M.; Schöning, M.: The development of cerebral perfusion during the first three years of life: Long-term follow-up study of cerebral blood flow volume measurement in two healthy children
P019
Stülpnagel, C. von; Gehrmann, A.; Roos, R.: Intracerebral calcification in a newborn – Not always a connatal infection
P020
Opladen, T.; Moog, U.; Hoffmann, G. F.: Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia
P021
Alber, M.; Bevot, A.; Stötter, M.; Horvath, R.; Krägeloh-Mann, I.: Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect
P022
Schwartz, O.; Denecke, J.; Fiedler, B.; Keyvani, K.; Kress, W.; Kurlemann, G.: A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
P023
Tacke, U.; Gerecke, A.; Uhl, M.; Korinthenberg, R.: Wernicke encephalopathy in childhood
P024
Korall, H.: Screening for pyridoxine dependent epilepsy (PDE) by Tandem Mass Spectrometry (HPLC-MS/MS)
P025
Mengel, E.; Koch, S.; Das, A.; Ebinger, F.; Hartung, R.; Korenke, C.; Marquardt, T.; Rutsch, F.; Tsiakas, K.; Harzer, K.: Manifestation and diagnosis of NPC disease in Germany
P026
Illsinger, S.; Lücke, T.; Hartmann, H.; Donnerstag, F.; Das, A. M.: M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
P027
Brunner-Krainz, M.; Achatz, E.; Wendelin, G.; Erwa, W.; Fowler, B.; Plecko, B.: Homocystein as an important diagnostic marker of remethylation defects – A case report
P028
Hahn, A.; Neubauer, B.; Hecker, A.; Hirschburger, M.; Motz, R.; Haase, C.; Marquardt, T.: Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease
P029
Hofer, D.; Paul, K.; Fantur, K.; Beck, M.; Ledvinova, J.; Michelakakis, H.; Plecko, B.; Paschke, E.: GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
P030
Albrecht, U.; Sergi, C.; Steichen-Gersdorf, E.; Gotwald, T.; Kotzot, D.; Vianey-Saban, C.; Haberlandt, E.; Karall, D.; Scholl-Bürgi, S.: Cardiac arrest in a patient with glutaric aciduria type II
P031
Lebrun, A. H.; Storch, S.; Kyttällä, A.; Mole, S. E.; Kohlschütter, A.; Kruse, B.; Ullrich, K.; Braulke, T.; Schulz, A.: Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
P032
Schlotawa, L.; Huppke, P.; Ludwig, H. C.; Steinfeld, R.; Klepper, J.; Gärtner, J.: Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
P033
Klein, A.; Rohrbach, M.; Scheer, I.; Balmer, C.; Baumgartner, M.; Boltshauser, E.: Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
P034
Eichholz, S.; Lorenz, N.; Kreuder, J.; Logeswaran, T.; Schranz, D.; Kabus, M.: Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
P035
Kehrer, C.; Opherk, K.; Müller, I.; Wilke, M.; Krägeloh-Mann, I.: Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)
P036
Böhmer, S.; Vester, U.; Schweiger, B.; Schaper, J.; Schara, U.: Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease
P037
Rhein, M. von; Habermehl, P.; Mengel, E.; Knuf, M.: Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia
P038
Fiedler, B. J.; Schwartz, O.; Abels, C.; Kurlemann, G.: Epilepsy in vitamin B12 deficiency and its treatment in infancy
P039
Haas-Lude, K.; Alber, M.; Lettau, M.; Krägeloh-Mann, I.: Neurocysticercosis in a 10 year-old boy in Germany
P040
Baumann, M.; Birnbacher, R.; Koch, J.; Strobl, R.; Rostasy, K.: Uncommon manifestations of childhood neuroborreliosis
P041
Bigi, S.; Aebi, C.; Steinlin, M.: Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood
P042
Maier, O.; Jäger, G.; Waibel, P.; Weissert, M.: Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report
P043
Scheffner, T.; Muckenhaupt, T.; Dütting, T.; Drosten, C.; Trefz, F. K.: Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases
P044
Prokop, K.; Smitka, M.; Hagen, M. von der; Hahn, G.; Ikonomidou, H.: Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?
P045
Rödl, S.; Marschitz, I.; Brunner-Krainz, M.; Sorantin, E.; Gruber-Sedlmayr, U.; Zobel, G.: 20 years evaluation of pediatric patients with encephalitis in the PICU
P046
Sengupta, D.; Bertsche, A.; Bast, T.; Vater, D.; Ebinger, F.: Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
P047
Elpers, C.; Stupp, N.; Grenzebach, U.; Niederstadt, T.; Allkemper, T.; Fiedler, B.; Schwartz, O.; Taeuber, A.; Kurlemann, G.: Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
P048
Schimmel, M.; Bien, C. G.; Vincent, A.; Schenk, W.; Walden, U.; Penzien, J.: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder
P049
Schlachter, K.; Ausserer, B.: Posterior reversible encephalopathy syndrome (PRES)
P050
Brunner-Krainz, M.; Pilhatsch, A.; Wendelin, G.; Eder, H. G.; Feichtinger, M.; Plecko, B.: Febrile seizures – First symptom of Rasmussenencephalitis
P051
Syrbe, S.; Bernhard, M. K.; Schulz, M.; Pernice, W.; Merkenschlager, A.: Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
P052
Frey, S. G.; Weber, P.; Datta, A. N.: Acute disseminated encephalomyelitis review in 8 pediatric patients
P053
Gröppel, G.; Dressler, A.; Freilinger, M.; Mayer, H.; Pahs, G.; Porsche, B.; Reiter, E.; Urak, L.; Czech, T.; Hainfellner, J.; Prayer, D.; Feucht, M.: Surgery during early life in children with intractable epilepsy – A prospective evaluation
P054
Högler, W.; Wudy, S.; Luef, G.; Hartmann, M.; Rauchenzauner, M.: Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
P055
Reutlinger, C.; Baudhuin, J. A.; Dreiwes, C.; Stephani, U.; Boor, R.: Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
P056
Koch, J.; Rauscher, C.: Treatment of West syndrome (WS) according to UKISS (United Kindom Infantile Spasms Study): A single centers experience
P057
Nomayo, H. O.: IV Levetiracetam in the management of refractory complex-partial status epilepticus
P058
Obermeier, T.; Helbig, I.; Spiczak, S. von; Boor, R.; Weber, Y.; Lerche, H.; Neubauer, B.; Franke, A.; Schreiber, S.; Stephani, U.; Muhle, H.: Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
P059
Syrbe, S.; Landgraf, M.; Bernhard, M. K.; Merkenschlager, A.: Toxic effects of lamotrigine ingestion in children
P060
Bernhard, M. K.; Uhlig, H.; Mütze, U.; Syrbe, S.; Miehe, U.; Merkenschlager, A.: Seizures caused by accidental dimenhydriante intoxication
P061
Rittinger, O.; Kornak, U.: Intractable seizures in malignant infantile osteopetrosis due to CLCN7 mutation: lysosomal aspects
P062
Oster, I.; Meyer, S.; Shamdeen, M. G.; Gortner, L.: The prognostic value of EEG in children with minor head trauma
P063
Bernhard, M. K.; Himpel, M.; Landgraf, M.; Syrbe, S.; Merkenschlager, A.: Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
P064
Grønborg, S.; Huppke, P.; Schramm, P.; Gärtner, J.; Brockmann, K.: Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy
P065
Jung, N. H.; Kuhnke, N.; Hauschke, D.; Stolle, S.; Delvendahl, I.; Mall, V.: Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?
P066
Poretti, A.; Rauscher, C.; Neuhann, T.; Forstner, R.; Hahn, G.; Koch, J.; Tinschert, S.; Boltshauser, E.: Pontine tegmental cap dysplasia: Two additional cases
P067
Poretti, A.; Limperopoulos, C.; Wolf, N. I.; Roulet-Perez, E.; Rauscher, C.; Prayer, D.; Müller, A.; Weissert, M.; Kotzaeridou, U.; du Plessis, A. J.; Huisman, T. A.; Boltshauser, E.: Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
P068
Sanchez-Albisua, I.; Merten, A.; Mayrhofer, H.; Grodd, W.; Krägeloh-Mann, I.: Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation
P069
Smitka, M.; Hahn, G.; Morris-Rosendahl, D. J.; Ikonomidou, C.; Hagen, M. von der: Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M
P070
Schröder, S. A.; Berweck, S.; Huß, K.; Borggraefe, I.; Heinen, F.: Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
P071
Berweck, S.; Schröder, S. A.; Huß, K.; Borggraefe, I.; Heinen, F.: Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
P072
Sprinz, A.; Dercks, M.; Weglage, J.; Nagel, A.: Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood
P073
Sprinz, A.; Nagel, A.: Multimodal treatment of Cerebral Palsy (CP) including physical therapy, Botulinumtoxin und Lokomat-Training: A case report
P074
Sprinz, A.; Nagel, A.; Dercks, M.; Illerhaus, M.; Weglage, J.: Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)
P075
Jung, N. H.; Heinen, F.; Reissig, A.; Westhoff, B.; Berweck, S.; Mall, V.: Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
P076
Nomayo, H. O.; Hahn, J.: Continous intrathecal baclofen (cITB) therapy terminates spinal spasms mimicking tonic seizures in a teenager with severe spastic cerebral palsy with total body involvement and cervical dystonia
P077
Huß, K.; Berweck, S.; Schröder, A. S.; Mall, V.; Borggräfe, I.; Heinen, F.: Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
P078
Zeiner, F.; Lütjen, S.; Holthausen, H.; Staudt, M.: Hemiplegic migraine with cerebellar atrophy: A second pediatric case
P079
Kim, K. S.; Kotzaeridou, U.; Seitz, A.; Schmitt, C. P.; Wolf, N.; Pietz, J.: Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report
P080
Gudegast, C.; Niesytto, C.; Fritsch, M. J.; Schröder, H. W. S.; Weigel, C.; Stenger, R. D.: Outcome of endoscopic therapy of complex hydrocephalus
P081
Utzig, N.; Davids, S.; Thoms, K.; Jagdhuhn, M.; Hirschfeld, H.; Domin, M.; Hamm, A.; Lotze, M.; Lauffer, H.: Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
P082
Müller, H. L.; Schröder, S.; Gebhardt, U.; Zwiener, I.; Faldum, A.; Warmuth-Metz, M.; Pietsch, T.; Kolb, R.; Wiegand, C.; Sörensen, N.: Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients
P083
Geis, T.; Schilling, S.: Tumor induced Hemichorea
P084
Müller, H. L.; Gebhardt, U.; Reinehr, T.; Enrion, P. J.; Cowley, M. A.; Roth, C. L.: Peripheral alpha MSH in childhood obesity and craniopharyngioma
P085
Gebhardt, U.; Schröder, S.; Pohl, F.; Kortmann, R. D.; Zwiener, I.; Faldum, A.; Warmuth-Metz, M.; Pietsch, T.; Calaminus, G.; Kolb, R.; Wiegand, C.; Sörensen, N.; Müller, H. L.: Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment
P086
Pansy, J.; Marschik, P. B.; Einspieler, C.: Associated movements in 5- to 10-year-old infants
P087
Rapp, E. M.; Marschik, P. B.; Pansy, J.; Einspieler, C.: Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?
P088
Pansy, J.; Einspieler, C.: Assessment of spontaneous movements in an infant with Peters anomaly
P089
Reuner, G.; Voigt, B.; Pauen, S.; Pietz, J.: Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“
P090
Schneider, C.; Krischke, G.; Walkinshaw, G.; Arend, M.; Rascher, W.; Trollmann, R.: Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)
P091
Hoffmann, L.; Kribs, A.; Jopp-Petzinna, G.: Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)
P092
Hawellek, N.; Hartmann, H.; Hoy, L.; Wedekin, M.; Lücke, T.; Das, A. M.; Illsinger, S.; Ehrich, J. H. H.; Pape, L.: Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
P093
Kim, K. S.; Wochner, K.; Karch, D.; Philippi, H.; Hadders-Algra, M.; Dickhaus, H.; Pietz, J.: Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)
P094
Rhein, M. von; Habermehl, P.; Schlee-Böckh, K.; Knuf, M.: Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature
P095
Juenemann, S.; Knecht, B.; Greiner, J.; Weissert, M.: Acute basilar artery thrombosis in childhood: A therapeutic dilemma
P096
Bigi, S.; Wehrli, E.; Steinlin, M.: Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation
P097
Lorenz, I.; Gratzki, N.; Wenzel, D.; Fahrig, A.; Ganslandt, O.; Trollmann, R.: Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
P098
Herbertz, S.; Kudernatsch, M.; Lehner, K.; Kluger, G.: Fast recovery after 5 months in persistent vegetative state
P099
Bernhard, M. K.; Syrbe, S.; Landgraf, M.; Merkenschlager, A.: Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
P100
Kotzaeridou, U.; Vater, D.; Ebinger, F.; Pietz, J.: Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report
P101
Neu, A.; Le, Q.; Hanganu, I.; Isbrandt, D.: KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
P102
Becher, T.; Weise, S.: Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate