Literature DB >> 34318393

Novel Homozygous Truncating Variant Widens the Spectrum of Early-Onset Multisystemic SYNE1 Ataxia.

William Kristian Karlsson1, Joan Lilja Sunnleyg Højgaard2, Anna Vilhelmsen3, Clarissa Crone4, Birgit Andersen4, Ian Law5, Lisbeth Birk Møller6, Troels Tolstrup Nielsen2,7, Emilie Neerup Nielsen2, Thomas Krag2,8, Kirsten Svenstrup2,8, Jørgen Erik Nielsen2,7.   

Abstract

Pathogenic variants in the SYNE1 gene are associated with a phenotypic spectrum spanning from late-onset, slowly progressive, relatively pure ataxia to early-onset, fast progressive multisystemic disease. Since its first description in 2007 as an adult-onset ataxia in French Canadian families, subsequent identification of patients worldwide has widened the clinical spectrum and increased the number of identified pathogenic variants. We report a 20-year-old Faroese female with early-onset progressive gait problems, weakness, dysphagia, slurred speech, orthostatic dizziness, and urge incontinence. Neurological examination revealed mild cognitive deficits, dysarthria, broken slow pursuit, hypometric saccades, weakness with spasticity, hyperreflexia, absent ankle reflexes, ataxia, and wide-based, spastic gait. Magnetic resonance imaging displayed atrophy of the cerebellum, brainstem, and spinal cord. Severely prolonged central motor conduction time and lower motor neuron involvement was demonstrated electrophysiologically. Fluorodeoxyglucose-positron emission tomography (FDG-PET) scan showed hypometabolism of the cerebellum and right frontal lobe. Muscle biopsy revealed chronic neurogenic changes and near-absent immunostaining for Nesprin-1. Next-generation sequencing revealed a previously undescribed homozygous truncating, likely pathogenic variant in the SYNE1 gene. The patient's mother and paternal grandfather were heterozygous carriers of the variant. Her father's genotype was unobtainable. We expand the list of likely pathogenic variants in SYNE1 ataxia with a novel homozygous truncating variant with proximity to the C-terminus and relate it to a phenotype comprising early-onset cerebellar deficits, upper and lower motor neuron involvement and cognitive deficits. Also, we report novel findings of focally reduced frontal lobe FDG-PET uptake and motor evoked potential abnormalities suggestive of central demyelination.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Ataxia; Autosomal recessive; Cerebellum; Nesprin; SYNE1; Spinocerebellar ataxia

Mesh:

Substances:

Year:  2021        PMID: 34318393     DOI: 10.1007/s12311-021-01308-w

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  11 in total

1.  Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands.

Authors:  Thomas D Als; Tove H Jorgensen; Anders D Børglum; Peter A Petersen; Ole Mors; August G Wang
Journal:  Eur J Hum Genet       Date:  2006-04       Impact factor: 4.246

Review 2.  The autosomal recessive cerebellar ataxias.

Authors:  Mathieu Anheim; Christine Tranchant; Michel Koenig
Journal:  N Engl J Med       Date:  2012-02-16       Impact factor: 91.245

3.  Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants.

Authors:  Xiaohui Duan; Ying Hao; Zhenhua Cao; Chao Zhou; Jin Zhang; Renbin Wang; Shaojie Sun; Weihong Gu
Journal:  Cerebellum       Date:  2020-09-05       Impact factor: 3.847

4.  SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.

Authors:  Matthis Synofzik; Katrien Smets; Martial Mallaret; Daniela Di Bella; Constanze Gallenmüller; Jonathan Baets; Martin Schulze; Stefania Magri; Elisa Sarto; Mona Mustafa; Tine Deconinck; Tobias Haack; Stephan Züchner; Michael Gonzalez; Dagmar Timmann; Claudia Stendel; Thomas Klopstock; Alexandra Durr; Christine Tranchant; Marc Sturm; Wahiba Hamza; Lorenzo Nanetti; Caterina Mariotti; Michel Koenig; Ludger Schöls; Rebecca Schüle; Peter de Jonghe; Mathieu Anheim; Franco Taroni; Peter Bauer
Journal:  Brain       Date:  2016-04-17       Impact factor: 13.501

5.  Multimodal neuroimaging analysis in patients with SYNE1 Ataxia.

Authors:  Maria T D Gama; Camila C Piccinin; Thiago J R Rezende; Patrick A Dion; Guy A Rouleau; Marcondes C França Junior; Orlando G P Barsottini; José Luiz Pedroso
Journal:  J Neurol Sci       Date:  2018-05-04       Impact factor: 3.181

6.  Scale for the assessment and rating of ataxia: development of a new clinical scale.

Authors:  T Schmitz-Hübsch; S Tezenas du Montcel; L Baliko; J Berciano; S Boesch; C Depondt; P Giunti; C Globas; J Infante; J-S Kang; B Kremer; C Mariotti; B Melegh; M Pandolfo; M Rakowicz; P Ribai; R Rola; L Schöls; S Szymanski; B P van de Warrenburg; A Dürr; T Klockgether; Roberto Fancellu
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

7.  Cognitive impairment in ARCA-1, a newly discovered pure cerebellar ataxia syndrome.

Authors:  Robert Laforce; James P Buteau; Jean-Pierre Bouchard; Guy A Rouleau; Rémi W Bouchard; Nicolas Dupré
Journal:  Cerebellum       Date:  2010-09       Impact factor: 3.847

8.  Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation.

Authors:  Matthias Baumann; Elisabeth Steichen-Gersdorf; Birgit Krabichler; Britt-Sabina Petersen; Ulrike Weber; Wolfgang M Schmidt; Johannes Zschocke; Thomas Müller; Reginald E Bittner; Andreas R Janecke
Journal:  Eur J Hum Genet       Date:  2016-10-26       Impact factor: 4.246

9.  Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

Authors:  François Gros-Louis; Nicolas Dupré; Patrick Dion; Michael A Fox; Sandra Laurent; Steve Verreault; Joshua R Sanes; Jean-Pierre Bouchard; Guy A Rouleau
Journal:  Nat Genet       Date:  2006-12-10       Impact factor: 38.330

10.  Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrum.

Authors:  Inès Mademan; Florian Harmuth; Ilaria Giordano; Dagmar Timmann; Stefania Magri; Tine Deconinck; Jens Claaßen; Daniel Jokisch; Gencer Genc; Daniela Di Bella; Silvia Romito; Rebecca Schüle; Stephan Züchner; Franco Taroni; Thomas Klockgether; Ludger Schöls; Peter De Jonghe; Peter Bauer; Eoa Consortium; Jonathan Baets; Matthis Synofzik
Journal:  Brain       Date:  2016-05-19       Impact factor: 13.501

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