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Autor(en) / Beteiligte
Titel
How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey
Ist Teil von
  • European journal of neurology, 2022-07, Vol.29 (7), p.1885-1891
Ort / Verlag
England: John Wiley & Sons, Inc
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Wiley Online Journals
Beschreibungen/Notizen
  • Background and purpose Seven thousand rare diseases have been identified; most of them are of genetic origin. The diagnosis of a neurogenetic disease is difficult, and management and training programs are not well defined through Europe. To capture and assess care needs, the Neurogenetics Panel of the European Academy of Neurology (EAN) has performed an explorative survey. Methods The survey covering multiple topics of neurogenetics was sent to all neurologists and neuropediatricians affiliated with the EAN practicing in Europe. Results We collected answers from 239 members based in 40 European member states. Even though most of the responders were aware of neurogenetic diseases, when we came to amenability of carrying out a complete genetic diagnosis, almost one‐third of the responders declared they were not happy with the current way of ordering genetic analyses in their countries. Furthermore, although single‐gene analysis is diffusely present in Europe, whole exome and genome sequencing are not easily accessible, with considerable variabilities among countries. Almost 10% of the responders did not know if presymptomatic and prenatal diagnosis was available in their countries, and 47.3% were not aware of which newborn screening programs were available. Finally, 96.3% of responders declared that there is a need for education and training in neurogenetics. Conclusions We believe that this survey may be of importance for all European stakeholders in neurogenetics in identifying key priorities, targeting areas to encourage education/travel fellowships, and educational seminars in the future, because this area will only accelerate, and diagnostic requirements will expand. The diagnosis of a neurogenetic disease is difficult, and management and training programs are not well defined through Europe. To capture and assess care needs, the Neurogenetics Panel of the European Academy of Neurology has performed an explorative survey. We believe that this survey may be of importance for all European stakeholders in neurogenetics in identifying key priorities.
Sprache
Englisch
Identifikatoren
ISSN: 1351-5101
eISSN: 1468-1331
DOI: 10.1111/ene.15320
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9314134

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