Literature DB >> 26377695

Non-Ataxic Presenting Symptoms of Dominant Ataxias.

Elsdon Storey1,2.   

Abstract

While the onset of a dominantly inherited ataxia is typically taken to be the onset of gait ataxia, a wide range of other symptoms related to central and/or peripheral nervous system impairment, or even to non-neurological involvement, can be the presenting feature. Knowledge of these is fairly robust for the commonest spinocerebellar ataxias (SCAs 1, 2, 3 and 6) and for those where a striking non-ataxic presentation is the norm (SCAs 7 and 12), but the literature is potentially misleading in the rarer dominant ataxias. This review summarises what is currently known of these non-ataxic presentations and outlines and explains the difficulties associated with determining non-ataxic presentations of dominant ataxias. The relevant literature was surveyed, including systematic reviews (where available) and case reports. Non-ataxic presentations of dominant ataxias are classified by symptom.

Entities:  

Keywords:  Clinical presentation; Dominant ataxias; SCAs; Spinocerebellar ataxias

Mesh:

Year:  2016        PMID: 26377695     DOI: 10.1007/s12311-015-0721-5

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


  29 in total

1.  Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.

Authors:  P Bauer; F Laccone; A Rolfs; U Wüllner; S Bösch; H Peters; S Liebscher; M Scheible; J T Epplen; B H F Weber; E Holinski-Feder; H Weirich-Schwaiger; D J Morris-Rosendahl; J Andrich; O Riess
Journal:  J Med Genet       Date:  2004-03       Impact factor: 6.318

2.  Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.

Authors:  Esther Brusse; Inge de Koning; Anneke Maat-Kievit; Ben A Oostra; Peter Heutink; John C van Swieten
Journal:  Mov Disord       Date:  2006-03       Impact factor: 10.338

3.  Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.

Authors:  Michael F Waters; Natali A Minassian; Giovanni Stevanin; Karla P Figueroa; John P A Bannister; Dagmar Nolte; Allan F Mock; Virgilio Gerald H Evidente; Dominic B Fee; Ulrich Müller; Alexandra Dürr; Alexis Brice; Diane M Papazian; Stefan M Pulst
Journal:  Nat Genet       Date:  2006-02-26       Impact factor: 38.330

4.  Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.

Authors:  Karen N McFarland; Jilin Liu; Ivette Landrian; Desmond Zeng; Salmo Raskin; Mariana Moscovich; Emilia M Gatto; Adriana Ochoa; Hélio A G Teive; Astrid Rasmussen; Tetsuo Ashizawa
Journal:  Neurogenetics       Date:  2013-12-07       Impact factor: 2.660

5.  Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.

Authors:  Zoran Brkanac; Magali Fernandez; Mark Matsushita; Hilary Lipe; John Wolff; Thomas D Bird; Wendy H Raskind
Journal:  Am J Med Genet       Date:  2002-05-08

6.  Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

Authors:  Raji P Grewal; Madhureeta Achari; Tohru Matsuura; Alberto Durazo; Emilio Tayag; Lan Zu; Stefan M Pulst; Tetsuo Ashizawa
Journal:  Arch Neurol       Date:  2002-08

7.  Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.

Authors:  J-Y Kim; S Y Kim; J-M Kim; Y K Kim; K-Y Yoon; J Y Kim; B C Lee; J S Kim; S H Paek; S S Park; S E Kim; B S Jeon
Journal:  Neurology       Date:  2009-04-21       Impact factor: 9.910

8.  Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Authors:  Heike Jacobi; Kathrin Reetz; Sophie Tezenas du Montcel; Peter Bauer; Caterina Mariotti; Lorenzo Nanetti; Maria Rakowicz; Anna Sulek; Alexandra Durr; Perrine Charles; Alessandro Filla; Antonella Antenora; Ludger Schöls; Julia Schicks; Jon Infante; Jun-Suk Kang; Dagmar Timmann; Roberto Di Fabio; Marcella Masciullo; Laszlo Baliko; Bela Melegh; Sylvia Boesch; Katrin Bürk; Annkathrin Peltz; Jörg B Schulz; Isabelle Dufaure-Garé; Thomas Klockgether
Journal:  Lancet Neurol       Date:  2013-05-22       Impact factor: 44.182

Review 9.  Nonmotor and extracerebellar features in Machado-Joseph disease: a review.

Authors:  José Luiz Pedroso; Marcondes C França; Pedro Braga-Neto; Anelyssa D'Abreu; Maria Luiza Saraiva-Pereira; Jonas A Saute; Hélio A Teive; Paulo Caramelli; Laura Bannach Jardim; Iscia Lopes-Cendes; Orlando Graziani P Barsottini
Journal:  Mov Disord       Date:  2013-06-17       Impact factor: 10.338

10.  'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.

Authors:  María García-Murias; Beatriz Quintáns; Manuel Arias; Ana I Seixas; Pilar Cacheiro; Rosa Tarrío; Julio Pardo; María J Millán; Susana Arias-Rivas; Patricia Blanco-Arias; Dolores Dapena; Ramón Moreira; Francisco Rodríguez-Trelles; Jorge Sequeiros; Angel Carracedo; Isabel Silveira; María J Sobrido
Journal:  Brain       Date:  2012-04-03       Impact factor: 13.501

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  2 in total

1.  Cerebellum: from Fundamentals to Translational Approaches. The Seventh International Symposium of the Society for Research on the Cerebellum.

Authors:  Mario Manto; Peter Mariën
Journal:  Cerebellum       Date:  2016-02       Impact factor: 3.847

2.  Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population.

Authors:  Szu-Ju Chen; Ni-Chung Lee; Yin-Hsiu Chien; Wuh-Liang Hwu; Chin-Hsien Lin
Journal:  Brain Behav       Date:  2019-09-16       Impact factor: 2.708

  2 in total

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