47 patients with FLNA associated periventricular nodular heterotopia

被引:0
|
作者
Max Lange
Burkhard Kasper
Axel Bohring
Frank Rutsch
Gerhard Kluger
Sabine Hoffjan
Stephanie Spranger
Anne Behnecke
Andreas Ferbert
Andreas Hahn
Barbara Oehl-Jaschkowitz
Luitgard Graul-Neumann
Katharina Diepold
Isolde Schreyer
Matthias K. Bernhard
Franziska Mueller
Ulrike Siebers-Renelt
Ana Beleza-Meireles
Goekhan Uyanik
Sandra Janssens
Eugen Boltshauser
Juergen Winkler
Gerhard Schuierer
Ute Hehr
机构
[1] University of Regensburg,Department of Neurosurgery
[2] Medical Center,Department of Neurology
[3] Epilepsy Center,Department of General Pediatrics
[4] University of Erlangen,Department of Pediatrics
[5] Medical Center,Division of Neuropediatrics
[6] Institute of Human Genetics,Division of Molecular Neurology
[7] University of Muenster,Department of Neuroradiology
[8] Muenster University Children’s Hospital,Department of Human Genetics
[9] Neuropädiatrie,undefined
[10] Schön Klinik Vogtareuth,undefined
[11] Vogtareuth,undefined
[12] Germany und Paracelsus Medical University,undefined
[13] Salzburg/Austria,undefined
[14] Department of Human Genetics,undefined
[15] Ruhr-University Bochum,undefined
[16] Praxis fuer Humangenetik,undefined
[17] Klinikum Bremen-Mitte,undefined
[18] Institute of Human Genetics,undefined
[19] Heidelberg University,undefined
[20] Klinik für Neurologie,undefined
[21] Klinikum Kassel and Medical School,undefined
[22] Department of Neuropediatrics,undefined
[23] University of Giessen,undefined
[24] Praxis fuer Humangenetik,undefined
[25] Ambulantes Gesundheitszentrum der Charité (Humangenetik),undefined
[26] Universitätsmedizin Berlin,undefined
[27] Department of Neuropediatrics,undefined
[28] Klinikum Kassel,undefined
[29] Institut für Humangenetik,undefined
[30] Uni Jena,undefined
[31] University of Leipzig Medical Center,undefined
[32] Center for Human Genetics,undefined
[33] Genetics Clinic,undefined
[34] Guy’s Hospital,undefined
[35] Guy’s and St Thomas’ NHS Foundation Trust,undefined
[36] Zentrum für Medizinische Genetik,undefined
[37] Hanusch-Krankenhaus der Wiener Gebietskrankenkasse,undefined
[38] Centre for Medical Genetics,undefined
[39] Ghent University Hospital,undefined
[40] University Children’s Hospital Zürich,undefined
[41] University Hospital,undefined
[42] Friedrich-Alexander-University Erlangen-Nuernberg,undefined
[43] University of Regensburg,undefined
[44] Medical Center,undefined
[45] University of Regensburg,undefined
[46] Medical Center,undefined
关键词
Periventricular nodular heterotopia; Filamin A; Imaging; Score; Seizures; Phenotype;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [1] 47 patients with FLNA associated periventricular nodular heterotopia
    Lange, Max
    Kasper, Burkhard
    Bohring, Axel
    Rutsch, Frank
    Kluger, Gerhard
    Hoffjan, Sabine
    Spranger, Stephanie
    Behnecke, Anne
    Ferbert, Andreas
    Hahn, Andreas
    Oehl-Jaschkowitz, Barbara
    Graul-Neumann, Luitgard
    Diepold, Katharina
    Schreyer, Isolde
    Bernhard, Matthias K.
    Mueller, Franziska
    Siebers-Renelt, Ulrike
    Beleza-Meireles, Ana
    Uyanik, Goekhan
    Janssens, Sandra
    Boltshauser, Eugen
    Winkler, Juergen
    Schuierer, Gerhard
    Hehr, Ute
    ORPHANET JOURNAL OF RARE DISEASES, 2015, 10
  • [2] Three Generations of FLNA-Associated Periventricular Nodular Heterotopia
    Eisenbiegler, Grace E.
    Brown, Stephen A.
    CASE REPORTS IN NEUROLOGY, 2021, 13 (03) : 776 - 780
  • [3] Lung disease associated with periventricular nodular heterotopia and an FLNA mutation
    Masurel-Paulet, Alice
    Haan, Eric
    Thompson, Elizabeth M.
    Goizet, Cyril
    Thauvin-Robinet, Christel
    Tai, Andrew
    Kennedy, Declan
    Smith, Greg
    Khong, Teck Yee
    Sole, Guilhem
    Guerineau, Elodie
    Coupry, Isabelle
    Huet, Frederic
    Robertson, Stephen
    Faivre, Laurence
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2011, 54 (01) : 25 - 28
  • [4] FLNA genomic rearrangements cause periventricular nodular heterotopia
    Clapham, K. R.
    Yu, T. W.
    Ganesh, V. S.
    Barry, B.
    Chan, Y.
    Mei, D.
    Parrini, E.
    Funalot, B.
    Dupuis, L.
    Nezarati, M. M.
    du Souich, C.
    van Karnebeek, C.
    Guerrini, R.
    Walsh, C. A.
    NEUROLOGY, 2012, 78 (04) : 269 - 278
  • [5] Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation
    Liu, Wenyu
    An, Dongmei
    Niu, Running
    Gong, Qiyong
    Zhou, Dong
    NEUROIMAGE-CLINICAL, 2018, 17 : 109 - 114
  • [6] Hemizygous FLNA variant in West syndrome without periventricular nodular heterotopia
    Yoshitaka Hiromoto
    Yoshiteru Azuma
    Yuichi Suzuki
    Megumi Hoshina
    Yuri Uchiyama
    Satomi Mitsuhashi
    Satoko Miyatake
    Takeshi Mizuguchi
    Atsushi Takata
    Noriko Miyake
    Mitsuhiro Kato
    Naomichi Matsumoto
    Human Genome Variation, 7
  • [7] Hemizygous FLNA variant in West syndrome without periventricular nodular heterotopia
    Hiromoto, Yoshitaka
    Azuma, Yoshiteru
    Suzuki, Yuichi
    Hoshina, Megumi
    Uchiyama, Yuri
    Mitsuhashi, Satomi
    Miyatake, Satoko
    Mizuguchi, Takeshi
    Takata, Atsushi
    Miyake, Noriko
    Kato, Mitsuhiro
    Matsumoto, Naomichi
    HUMAN GENOME VARIATION, 2020, 7 (01)
  • [8] The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia
    Lu, Yan-Ting
    Hsu, Chung-Yao
    Liu, Yo-Tsen
    Chan, Chung -Kin
    Chuang, Yao-Chung
    Lin, Chih-Hsiang
    Chang, Kai-Ping
    Ho, Chen-Jui
    Ng, Ching -Ching
    Lim, Kheng-Seang
    Tsai, Meng -Han
    BIOMEDICAL JOURNAL, 2022, 45 (03) : 542 - 548
  • [9] Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy
    Fallil, Zianka
    Pardoe, Heath
    Bachman, Robert
    Cunningham, Benjamin
    Parulkar, Isha
    Shain, Catherine
    Poduri, Annapurna
    Knowlton, Robert
    Kuzniecky, Ruben
    EPILEPSY & BEHAVIOR, 2015, 51 : 321 - 327
  • [10] Atypical male and female presentations of FLNA-related periventricular nodular heterotopia
    Fergelot, Patricia
    Coupry, Isabelle
    Rooryck, Caroline
    Deforges, Julie
    Maurat, Elise
    Sole, Guilhem
    Boute, Odile
    Dieux-Coeslier, Anne
    David, Albert
    Marchal, Cecile
    Thambo, Jean-Benoit
    Lacombe, Didier
    Arveiler, Benoit
    Goizet, Cyril
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2012, 55 (05) : 313 - 318