DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 43 · April 2012 DOI: 10.1055/s-002-23054


Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics
Münster, 19th to 22nd April 2012

Chair: Prof. Dr. med. Gerhard Kurlemann, Münster
Abstracts (HTML) List of Authors
PS13_01
Thiels, C; Köhler, C; Weigt-Usinger, K; Sutter, C; Lücke, T: New mutation in TSC1-gene in a sporadic case with initially mild phenotype
PS13_02
Schmitz, N; Rost, I; König, R; Kieslich, M: A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features
PS13_03
Riess, A; Grasshoff, U; Hehr, U; Bonin, M: Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.
PS13_04
Böhringer, E; Datta, A; Miny, P; Filges, I: Mosaic ring chromosome 3 in a child with epilepsy and developmental delay
PS13_06
Nebgen, S; Zerres, K; Deutz, U; Wiesmann, M; Häusler, M: Bannayan-Riley-Ruvalcaba-syndrom – an unusual differential diagnosis of dilatated Virchow-Robin spaces
PS13_07
Schwerin-Nagel, A; Uhrig, S; Heitzer, E; Wagner, K; Gruber-Sedlmayr, U; Lindbichler, P; Brunner-Krainz, M: Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly
PS13_09
Rosenbaum, T; Wiater, A; Stahn, V; Jeibmann, A; Harder, A: Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis
PS13_10
Langer, S; Mainberger, F; Delvendahl, I; Mall, V: Attention deficit in patients with Noonan Syndrome (NS)
PS13_11
Tacke, U; Speckmann, C; Rieger-Fackeldey, E; Hentschel, R; Rückauer, K; Arnold, R; Lausch, E: Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms
PS13_12
Munteanu, M; Trippe, H; Albrecht, B; Barthelmie, A; Wieczorek, D; Schara, U: Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia