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270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands.
Abiusi, Emanuela; Costa-Roger, Mar; Bertini, Enrico Silvio; Tiziano, Francesco Danilo; Tizzano, Eduardo F; Abiusi, Emanuela; Baranello, Giovanni; Bertini, Enrico; Boemer, François; Burghes, Arthur; Codina-Solà, Marta; Costa-Roger, Mar; Dangouloff, Tamara; Groen, Ewout; Gos, Monika; Jedrzejowska, Maria; Kirschner, Janbernd; Lemmink, Henny H; Müller-Felber, Wolfgang; Ouillade, Marie-Christine; Quijano-Roy, Susana; Rucinski, Kacper; Saugier-Veber, Pascale; Tiziano, Francesco Danilo; Tizzano, Eduardo Fidel; Wirth, Brunhilde.
Afiliação
  • Abiusi E; Section of Genomic Medicine, Department of Public Health and Life Sciences, Università Cattolica del Sacro Cuore, Roma, Italy
  • Costa-Roger M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain
  • Bertini ES; Research Unit of Neuromuscular Disease, Bambino Gesu' Children's Hospital, IRCCS, Roma, Italy
  • Tiziano FD; Section of Genomic Medicine, Department of Public Health and Life Sciences, Università Cattolica del Sacro Cuore, Roma, Italy
  • Tizzano EF; Complex Unit of Medical Genetics, Fondazione Policlinico Universitario IRCCS "A. Gemelli", Roma, Italy
  • Baranello G; Section of Genomic Medicine, Dept. of Life Sciences and Public Health, Catholic University of the Sacred Heart, Roma, Italy
  • Bertini E; The Dubowitz Neuromuscular Centre, Developmental Neuroscience Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, NIHR Great Ormond Street Hospital Biomedical Research Centre & Great Ormond Street Hospital NHS Foundation Trust, 30 Guilford Street, London WC1N 1EH
  • Boemer F; Italy, Research Unit of Neuromuscular Disease, Bambino Gesù Children's Hospital, IRCCS, Roma, Italy
  • Burghes A; Biochemical Genetics Lab, Department of Human Genetics, University Hospital, University of Liège, 4000 Liège, Belgium
  • Codina-Solà M; Department of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, USA
  • Costa-Roger M; Neuromuscular Reference Center, Department of Paediatrics, University Hospital Liege & University of Liege, Belgium
  • Dangouloff T; Department of Neurology & Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands
  • Groen E; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
  • Gos M; Department of Neurology, Medical University of Warsaw, Warsaw, Poland
  • Jedrzejowska M; Department of Neuropediatrics and Muscle Disorders, Medical Center University of Freiburg, Faculty of Medicine, Freiburg, Germany
  • Kirschner J; Department of Genetics, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands
  • Lemmink HH; Centre for Neuromuscular Disorders, Center for Translational Neuro and Behavioral Sciences, Department of Pediatric Neurology, University Duisburg-Essen, 45147 Essen, Germany
  • Müller-Felber W; AFM Téléthon, Évry, France; SMA Europe; European Alliance for Newborn Screening in Spinal Muscular Atrophy
  • Ouillade MC; Pediatric Neuromuscular Unit (NEIDF Reference Center at FILNEMUS & Euro-NMD), Child Neurology Department, Raymond Poincaré Hospital (UVSQ), APHP Université Paris Saclay, Garches France
  • Quijano-Roy S; Fundacja SMA, Warsaw, Poland; SMA Europe; European Alliance for Newborn Screening in Spinal Muscular Atrophy
  • Rucinski K; Univ Rouen Normandie, Inserm U1245, Normandie Univ and CHU Rouen, Department of Genetics and Nord/Est/Ile de France Neuromuscular Reference Center, F-76000 Rouen, France
  • Saugier-Veber P; Institute of Medical Genomics, Dept. of Life Sciences and Public Health, Catholic University of the Sacred Heart, and Complex Unit of Medical Genetics, Fondazione Policlinico Universitario IRCCS "A. Gemelli", Roma, Italy
  • Tiziano FD; Institute of Human Genetics, University Hospital of Cologne, Center for Molecular Medicine, University of Cologne and Center for Rare Diseases Cologne, University Hopsital of Cologne, Cologne, Germany
  • Tizzano EF; Institute of Medical Genomics, Dept. of Life Sciences and Public Health, Catholic University of the Sacred Heart, and Complex Unit of Medical Genetics, Fondazione Policlinico Universitario IRCCS "A. Gemelli", Roma, Italy
  • Wirth B; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain
Neuromuscul Disord ; 34: 114-122, 2024 01.
Article em En | MEDLINE | ID: mdl-38183850
ABSTRACT
The 270th ENMC workshop aimed to develop a common procedure to optimize the reliability of SMN2 gene copy number determination and to reinforce collaborative networks between molecular scientists and clinicians. The workshop involved neuromuscular and clinical experts and representatives of patient advocacy groups and industry. SMN2 copy number is currently one of the main determinants for therapeutic decision in SMA patients participants discussed the issues that laboratories may encounter in this molecular test and the cruciality of the accurate determination, due the implications as prognostic factor in symptomatic patients and in individuals identified through newborn screening programmes. At the end of the workshop, the attendees defined a set of recommendations divided into four topics SMA molecular prognosis assessment, newborn screening for SMA, SMN2 copies and treatments, and modifiers and biomarkers. Moreover, the group draw up a series of recommendations for the companies manufacturing laboratory kits, that will help to minimize the risk of errors, regardless of the laboratories' expertise.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Proteína 2 de Sobrevivência do Neurônio Motor Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Proteína 2 de Sobrevivência do Neurônio Motor Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália