Action myoclonus — renal failure syndrome : characterization of a unique cerebro-renal disorder

Correspondence to: Eva Andermann, MD, PhD, FCCMG, Neurogenetics Unit, Room 127, Montreal Neurological Hospital and Institute, 3801 University Street, Montreal, Quebec H3A 2B4, Canada E-mail: eva.andermann@mcgill.ca Neurogenetics Unit and Epilepsy Service, Montreal Neurological Hospital and Institute, Department of Human Genetics, Department of Neurology and Neurosurgery, Department of Pediatrics and MRS Unit, McConnell Brain Imaging Center, McGill University, Département de Génetique Médicale, Hôpital Sainte-Justine, Montreal, Service de Neurologie, Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, British Columbia Neuropsychiatry Program, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada, Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Department of Pathology, Alfred Hospital, Department of Anatomical Pathology, Royal Melbourne Hospital, Department of Neurology, Royal Melbourne Hospital, Melbourne Victoria, Australia and Parkinson’s Disease and Other Movement Disorders Center, Mayo Clinic, Scottsdale, Arizona, USA, Universität Göttingen, Paracelsus-Elena-Klinik, Kassel, Max Planck Institut für Psychiatrie and Institute of Human Genetics, National Research Center, Munich, Germany, Instituto de Neurologia Pilar, Hospital N. S. Pilar, Curitiba, Brazil and Serviço de Anatomia Patológica, Hospital de São João, Porto, Portugal