TY - JOUR
T1 - 270th ENMC International Workshop
T2 - Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands
AU - Abiusi, Emanuela
AU - Costa-Roger, Mar
AU - Bertini, Enrico Silvio
AU - Tiziano, Francesco Danilo
AU - Tizzano, Eduardo F
AU - Abiusi, Emanuela
AU - Baranello, Giovanni
AU - Bertini, Enrico
AU - Boemer, François
AU - Burghes, Arthur
AU - Codina-Solà, Marta
AU - Costa-Roger, Mar
AU - Dangouloff, Tamara
AU - Groen, Ewout
AU - Gos, Monika
AU - Jędrzejowska, Maria
AU - Kirschner, Janbernd
AU - Lemmink, Henny H
AU - Müller-Felber, Wolfgang
AU - Ouillade, Marie-Christine
AU - Quijano-Roy, Susana
AU - Rucinski, Kacper
AU - Saugier-Veber, Pascale
AU - Tiziano, Francesco Danilo
AU - Tizzano, Eduardo Fidel
AU - Wirth, Brunhilde
N1 - Publisher Copyright:
© 2023
PY - 2024/1
Y1 - 2024/1
N2 - 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.
AB - 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.
KW - Biomarkers/analysis
KW - Consensus Development Conferences as Topic
KW - Gene Dosage
KW - Humans
KW - Muscular Atrophy, Spinal/diagnosis
KW - Prognosis
KW - Survival of Motor Neuron 2 Protein/genetics
UR - http://www.scopus.com/inward/record.url?scp=85182899322&partnerID=8YFLogxK
U2 - 10.1016/j.nmd.2023.12.008
DO - 10.1016/j.nmd.2023.12.008
M3 - Article
C2 - 38183850
SN - 0960-8966
VL - 34
SP - 114
EP - 122
JO - Neuromuscular Disorders
JF - Neuromuscular Disorders
ER -