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The European Reference Network for Rare Neurological Diseases

Authors :
Reinhard, Carola
Bachoud-Lévi, Anne-Catherine
Bäumer, Tobias
Bertini, Enrico
Brunelle, Alicia
Buizer, Annemieke I.
Federico, Antonio
Gasser, Thomas
Groeschel, Samuel
Hermanns, Sanja
Klockgether, Thomas
Krägeloh-Mann, Ingeborg
Landwehrmeyer, G. Bernhard
Leber, Isabelle
Macaya Ruiz, Alfons
Mariotti, Caterina
Meissner, Wassilios G.
Molnar, Maria Judit
Nonnekes, Jorik
Ortigoza Escobar, Juan Dario
Pérez-Dueñas, Belén
Renna Linton, Lori
Schöls, Ludger
Schuele, Rebecca
Tijssen, Marina A. J.
Vandenberghe, Rik
Volkmer, Anna
Wolf, Nicole I.
Graessner, Holm
Universitat Autònoma de Barcelona
Reinhard, Carola
Bachoud-Lévi, Anne-Catherine
Bäumer, Tobias
Bertini, Enrico
Brunelle, Alicia
Buizer, Annemieke I.
Federico, Antonio
Gasser, Thomas
Groeschel, Samuel
Hermanns, Sanja
Klockgether, Thomas
Krägeloh-Mann, Ingeborg
Landwehrmeyer, G. Bernhard
Leber, Isabelle
Macaya Ruiz, Alfons
Mariotti, Caterina
Meissner, Wassilios G.
Molnar, Maria Judit
Nonnekes, Jorik
Ortigoza Escobar, Juan Dario
Pérez-Dueñas, Belén
Renna Linton, Lori
Schöls, Ludger
Schuele, Rebecca
Tijssen, Marina A. J.
Vandenberghe, Rik
Volkmer, Anna
Wolf, Nicole I.
Graessner, Holm
Universitat Autònoma de Barcelona
Publication Year :
2021

Abstract

While rare diseases (RDs) are by definition of low prevalence, the total number of patients suffering from an RD is high, and the majority of them have neurologic manifestations, involving central, peripheral nerve, and muscle. In 2017, 24 European Reference Networks (ERNs), each focusing on a specific group of rare or low-prevalence complex diseases, were formed to improve the care for patients with an RD. One major aim is to have "the knowledge travel instead of the patient," which has been put into practice by the implementation of the Clinical Patient Management System (CPMS) that enables clinicians to perform pan-European virtual consultations. The European Reference Network for Rare Neurological Diseases (ERN-RND) provides an infrastructure for knowledge sharing and care coordination for patients affected by a rare neurological disease (RND) involving the most common central nervous system pathological conditions. It covers the following disease groups: (i) Cerebellar Ataxias and Hereditary Spastic Paraplegias; (ii) Huntington's disease and Other Choreas; (iii) Frontotemporal dementia; (iv) Dystonia, (non-epileptic) paroxysmal disorders, and Neurodegeneration with Brain Iron Accumulation; (v) Leukoencephalopathies; and (vi) Atypical Parkinsonian Syndromes. At the moment, it unites 32 expert centers and 10 affiliated partners in 21 European countries, as well as patient representatives, but will soon cover nearly all countries of the European Union as a result of the ongoing expansion process. Disease expert groups developed and consented on diagnostic flowcharts and disease scales to assess the different aspects of RNDs. ERN-RND has started to discuss diagnostically unclear patients in the CPMS, is one of four ERNs that serve as foundation of Solve-RD, and has established an RND training and education program. The network will facilitate trial readiness through the establishment of an ERN-RND registry with a minimal data of all patients seen at the ERN-RND cen

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1337029387
Document Type :
Electronic Resource