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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias
- 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)
- Subjects :
- Iron
Genetic Phenomena::Genetic Variation::Mutation [PHENOMENA AND PROCESSES]
Kinesins
Catalysis
Atàxia - Aspectes genètics
Inorganic Chemistry
cerebellar atrophy
gene panel
Other subheadings::Other subheadings::/genetics [Other subheadings]
Humans
movement disorders
ataxia
neurodegeneration with brain iron accumulation (NBIA)
exome sequencing
Physical and Theoretical Chemistry
Molecular Biology
fenómenos genéticos::variación genética::mutación [FENÓMENOS Y PROCESOS]
Spectroscopy
Movement Disorders
Otros calificadores::Otros calificadores::/genética [Otros calificadores]
Organic Chemistry
Brain
Neurodegenerative Diseases
General Medicine
Computer Science Applications
Fenotip
Phosphotransferases (Alcohol Group Acceptor)
Anomalies cromosòmiques
Phenotype
enfermedades del sistema nervioso::manifestaciones neurológicas::discinesias::ataxia [ENFERMEDADES]
Mutation
Genetic Phenomena::Phenotype [PHENOMENA AND PROCESSES]
Ataxia
fenómenos genéticos::fenotipo [FENÓMENOS Y PROCESOS]
Nervous System Diseases::Neurologic Manifestations::Dyskinesias::Ataxia [DISEASES]
Subjects
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