Literature DB >> 23911094

Primary dystonias and genetic disorders with dystonia as clinical feature of the disease.

Narges Moghimi1, Bahman Jabbari2, Anna M Szekely3.   

Abstract

Dystonia is probably the most common form of movement disorder encountered in the clinical practice. It is characterized by sustained muscle contractions, usually producing twisting and repetitive movements or abnormal postures or positions. Dystonias can be classified in several ways, including primarily by the clinical phenomenology or by the underlining etiology, in particular to understand if the presentation is genetically determined. By advances of genetics, including contemporary genomic technologies, there is a growing understanding of the molecular underpinnings of genetically determined dystonias. The intricacy of information requires a user friendly, novel database that may efficiently serve clinicians to inform of advances of the field and to diagnose and manage these often complex cases. Here we present an up to date, comprehensive review - in tabulated formats - of genetically determined primary dystonias and complex Mendelian disorders with dystonia as central feature. The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features. We organized the findings not only by individual information (name of the conditions, pattern of inheritance, chromosome and gene abnormality, clinical features, relevant ancillary tests and key references), but also provide symptom-oriented organization of the clinical entities for efficient inquiries.
Copyright © 2013 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Dystonia; Gene table; Genetics; Review

Mesh:

Year:  2013        PMID: 23911094     DOI: 10.1016/j.ejpn.2013.05.015

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  5 in total

1.  Huntington's Disease Revealed by Familial Cervical Dystonia.

Authors:  Daniela Andriuta; Mélissa Tir; Olivier Godefroy; Pierre Krystkowiak
Journal:  Mov Disord Clin Pract       Date:  2016-01-18

Review 2.  Understanding the anatomy of dystonia: determinants of penetrance and phenotype.

Authors:  Renata P Lerner; Martin Niethammer; David Eidelberg
Journal:  Curr Neurol Neurosci Rep       Date:  2013-11       Impact factor: 5.081

Review 3.  Deep brain stimulation for dystonia: a novel perspective on the value of genetic testing.

Authors:  H A Jinnah; Ron Alterman; Christine Klein; Joachim K Krauss; Elena Moro; Marie Vidailhet; Robert Raike
Journal:  J Neural Transm (Vienna)       Date:  2017-02-03       Impact factor: 3.575

4.  Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism.

Authors:  Rachel Fremont; Ambika Tewari; Kamran Khodakhah
Journal:  Neurobiol Dis       Date:  2015-06-17       Impact factor: 5.996

5.  Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes.

Authors:  Natalie M Frederick; Parth V Shah; Alessandro Didonna; Monica R Langley; Anumantha G Kanthasamy; Puneet Opal
Journal:  Hum Mol Genet       Date:  2019-04-15       Impact factor: 6.150

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.