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September 18, 2012; 79 (12) Articles

Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis

Tiziana Pisano, A. James Barkovich, Richard J. Leventer, Waney Squier, Ingrid E. Scheffer, Elena Parrini, Susan Blaser, Carla Marini, Stephen Robertson, Gaetano Tortorella, Felix Rosenow, Pierre Thomas, George McGillivray, Eva Andermann, Frederick Andermann, Samuel F. Berkovic, William B. Dobyns, Renzo Guerrini
First published August 22, 2012, DOI: https://doi.org/10.1212/WNL.0b013e31826aac88
Tiziana Pisano
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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A. James Barkovich
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Richard J. Leventer
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Waney Squier
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Ingrid E. Scheffer
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Elena Parrini
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Susan Blaser
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Carla Marini
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Stephen Robertson
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Gaetano Tortorella
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Felix Rosenow
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Pierre Thomas
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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George McGillivray
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Eva Andermann
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Frederick Andermann
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Samuel F. Berkovic
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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William B. Dobyns
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Renzo Guerrini
From the Pediatric Neurology and Neurogenetics Unit (T.P., E.P., C.M., R.G.), Children's Hospital A. Meyer-University of Florence, Florence, Italy; Department of Radiology (A.J.B.), University of California, San Francisco; Children's Neuroscience Centre (R.J.L.), Murdoch Childrens Research Institute, University of Melbourne Department of Paediatrics, The Royal Children's Hospital, Melbourne, Australia; Paediatric Neurology Unit (W.S.), John Radcliffe Hospital, Oxford, UK; Epilepsy Research Centre (I.E.S., S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Melbourne; Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Melbourne, Australia; Diagnostic Imaging (S.B.), The Hospital for Sick Children, University of Toronto, Toronto, Canada; Department of Paediatrics and Child Health (S.R.), Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; Unit of Infantile Neuropsychiatry (G.T.), Department of Medical and Surgical Pediatrics, University Hospital of Messina, Messina, Italy; Department of Neurology (F.R.), Epilepsy Center Hessen, UKGM, Campus Marburg, Philipps-University Marburg, Germany; Unite Fonctionnelle EEG-Epileptologie (P.T.), Service de Neurologie, Hopital Pasteur, Nice, France; Genetic Health Services Victoria (G.M.), Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia; Montreal Neurological Hospital and Institute (E.A., F.A.), McGill University, Montreal, Canada; Seattle Children's Research Institute Center for Integrative Brain Research (W.B.D.), Seattle, WA; and Research Institute IRCCS ‘Stella Maris' Foundation (R.G.), Pisa, Italy.
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Citation
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis
Tiziana Pisano, A. James Barkovich, Richard J. Leventer, Waney Squier, Ingrid E. Scheffer, Elena Parrini, Susan Blaser, Carla Marini, Stephen Robertson, Gaetano Tortorella, Felix Rosenow, Pierre Thomas, George McGillivray, Eva Andermann, Frederick Andermann, Samuel F. Berkovic, William B. Dobyns, Renzo Guerrini
Neurology Sep 2012, 79 (12) 1244-1251; DOI: 10.1212/WNL.0b013e31826aac88

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Abstract

Objective: To describe a homogeneous subtype of periventricular nodular heterotopia (PNH) as part of a newly defined malformation complex.

Methods: Observational study including review of brain MRI and clinical findings of a cohort of 50 patients with PNH in the temporo-occipital horns and trigones, mutation analysis of the FLNA gene, and anatomopathologic study of a fetal brain.

Results: There were 28 females and 22 males. All were sporadic with the exception of an affected mother and son. Epilepsy occurred in 62%, cerebellar signs in 56%, cognitive impairment in 56%, and autism in 12%. Seventy percent were referred within the 3rd year of life. Imaging revealed a normal cerebral cortex in 76% and abnormal cortical folding in 24%. In all patients the hippocampi were under-rotated and in 10% they merged with the heterotopia. Cerebellar dysgenesis was observed in 84% and a hypoplastic corpus callosum in 60%. There was no gender bias or uneven gender distribution of clinical and anatomic severity. No mutations of FLNA occurred in 33 individuals examined. Heterotopia in the fetal brain revealed cytoarchitectonic characteristics similar to those associated with FLNA mutations; cortical pathology was not typical of polymicrogyria. Cerebellar involvement was more severe and the hippocampi appeared simple and under-rotated.

Conclusions: This series delineates a malformation complex in which PNH in the trigones and occipito-temporal horns is associated with hippocampal, corpus callosum, and cerebellar dysgenesis. This subtype of PNH is distinct from classic PNH caused by FLNA mutations.

GLOSSARY

BPNH =
bilateral periventricular nodular heterotopia;
dHPLC =
denaturing high-performance liquid chromatography;
DSM-IV =
Diagnostic and Statistical Manual of Mental Disorders, 4th edition;
PNH =
periventricular nodular heterotopia;
WAIS =
Wechsler Adult Intelligence Scale–Revised

Footnotes

  • Editorial, page 1192

  • Received November 11, 2011.
  • Accepted February 29, 2012.
  • Copyright © 2012 by AAN Enterprises, Inc.
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