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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

Authors :
Dolores Martínez-Rubio
Isabel Hinarejos
Paula Sancho
Nerea Gorría-Redondo
Raquel Bernadó-Fonz
Cristina Tello
Clara Marco-Marín
Itxaso Martí-Carrera
María Jesús Martínez-González
Ainhoa García-Ribes
Raquel Baviera-Muñoz
Isabel Sastre-Bataller
Irene Martínez-Torres
Anna Duat-Rodríguez
Patrícia Janeiro
Esther Moreno
Leticia Pías-Peleteiro
Mar O’Callaghan Gordo
Ángeles Ruiz-Gómez
Esteban Muñoz
Maria Josep Martí
Ana Sánchez-Monteagudo
Candela Fuster
Amparo Andrés-Bordería
Roser Maria Pons
Silvia Jesús-Maestre
Pablo Mir
Vincenzo Lupo
Belén Pérez-Dueñas
Alejandra Darling
Sergio Aguilera-Albesa
Carmen Espinós
Institut Català de la Salut
[Martínez-Rubio D, Hinarejos I] Rare Neurodegenerative Diseases Laboratory, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain. Joint Unit CIPF-IIS La Fe Rare Diseases, Valencia, Spain. [Sancho P, Tello C] Rare Neurodegenerative Diseases Laboratory, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain. [Gorría-Redondo N, Bernadó-Fonz R] Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitario de Navarra, Navarrabiomed, Pamplona, Spain. [Pérez-Dueñas B] Servei de Neurologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain
Vall d'Hebron Barcelona Hospital Campus
Instituto de Salud Carlos III
European Commission
Fundació La Marató de TV3
Generalitat Valenciana
Ministerio de Educación, Cultura y Deporte (España)
Fundació per Amor a L'Art
Marco-Marín, Clara [0000-0002-8813-3515]
Marco-Marín, Clara
Source :
International Journal of Molecular Sciences; Volume 23; Issue 19; Pages: 11847, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe, instname, Scientia, r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF), Universitat Rovira i virgili (URV), Digital.CSIC. Repositorio Institucional del CSIC
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

26 páginas, 4 figuras, 3 tablas<br />Our clinical series comprises 124 patients with movement disorders (MDs) and/or ataxia with cerebellar atrophy (CA), many of them showing signs of neurodegeneration with brain iron accumulation (NBIA). Ten NBIA genes are accepted, although isolated cases compatible with abnormal brain iron deposits are known. The patients were evaluated using standardised clinical assessments of ataxia and MDs. First, NBIA genes were analysed by Sanger sequencing and 59 patients achieved a diagnosis, including the detection of the founder mutation PANK2 p.T528M in Romani people. Then, we used a custom panel MovDisord and/or exome sequencing; 29 cases were solved with a great genetic heterogeneity (34 different mutations in 23 genes). Three patients presented brain iron deposits with Fe-sensitive MRI sequences and mutations in FBXO7, GLB1, and KIF1A, suggesting an NBIA-like phenotype. Eleven patients showed very early-onset ataxia and CA with cortical hyperintensities caused by mutations in ITPR1, KIF1A, SPTBN2, PLA2G6, PMPCA, and PRDX3. The novel variants were investigated by structural modelling, luciferase analysis, transcript/minigenes studies, or immunofluorescence assays. Our findings expand the phenotypes and the genetics of MDs and ataxias with early-onset CA and cortical hyperintensities and highlight that the abnormal brain iron accumulation or early cerebellar gliosis may resembling an NBIA phenotype.<br />This work was supported by the Instituto de Salud Carlos III (ISCIII)—Subdirección General de Evaluación y Fomento de la Investigación within the framework of the National R + D+I Plan co-funded with European Regional Development Funds (ERDF) [Grants PI18/00147 and PI21/00103 to CE]; the Fundació La Marató TV3 [Grants 20143130 and 20143131 to BPD and CE]; and by the Generalitat Valenciana [Grant PROMETEO/2018/135 to CE]. Part of the equipment employed in this work was funded by Generalitat Valenciana and co-financed with ERDF (OP ERDF of Comunitat Valenciana 2014–2020). PS had an FPU-PhD fellowship funded by the Spanish Ministry of Education, Culture and Sport [FPU15/00964]. IH has a PFIS-PhD fellowship [FI19/00072]. ASM has a contract funded by the Spanish Foundation Per Amor a l’Art (FPAA)

Details

ISSN :
14220067
Volume :
23
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....c2e20b8744f3e03b982dab5cae1b37d9
Full Text :
https://doi.org/10.3390/ijms231911847