Literature DB >> 27257945

Recent advances in genetics of chorea.

Niccolò E Mencacci1, Miryam Carecchio.   

Abstract

PURPOSE OF REVIEW: Chorea presenting in childhood and adulthood encompasses several neurological disorders, both degenerative and nonprogressive, often with a genetic basis. In this review, we discuss how modern genomic technologies are expanding our knowledge of monogenic choreic syndromes and advancing our insight into the molecular mechanisms responsible for chorea. RECENT
FINDINGS: A genome-wide association study in Huntington's disease identified genetic disease modifiers involved in controlling DNA repair mechanisms and stability of the HTT trinucleotide repeat expansion. Chorea is the cardinal feature of newly recognized genetic entities, ADCY5 and PDE10A-related choreas, with onset in infancy and childhood. A phenotypic overlap between chorea, ataxia, epilepsy, and neurodevelopmental disorders is becoming increasingly evident.
SUMMARY: The differential diagnosis of genetic conditions presenting with chorea has considerably widened, permitting a molecular diagnosis and an improved prognostic definition in an expanding number of cases. The identification of Huntington's disease genetic modifiers and new chorea-causing gene mutations has allowed the initial recognition of converging molecular pathways underlying medium spiny neurons degeneration and dysregulation of normal development and activity of basal ganglia circuits. Signalling downstream of dopamine receptors and control of cAMP levels represent a very promising target for the development of new aetiology-based treatments for chorea and other hyperkinetic disorders.

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Mesh:

Year:  2016        PMID: 27257945      PMCID: PMC4934600          DOI: 10.1097/WCO.0000000000000352

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  83 in total

Review 1.  Genetic modifiers of Huntington's disease.

Authors:  James F Gusella; Marcy E MacDonald; Jong-Min Lee
Journal:  Mov Disord       Date:  2014-08-25       Impact factor: 10.338

2.  Huntington disease phenocopy is a familial prion disease.

Authors:  R C Moore; F Xiang; J Monaghan; D Han; Z Zhang; L Edström; M Anvret; S B Prusiner
Journal:  Am J Hum Genet       Date:  2001-10-09       Impact factor: 11.025

Review 3.  Huntington's disease: from molecular pathogenesis to clinical treatment.

Authors:  Christopher A Ross; Sarah J Tabrizi
Journal:  Lancet Neurol       Date:  2011-01       Impact factor: 44.182

4.  Genotype-phenotype relationships in ataxia-telangiectasia and variants.

Authors:  S Gilad; L Chessa; R Khosravi; P Russell; Y Galanty; M Piane; R A Gatti; T J Jorgensen; Y Shiloh; A Bar-Shira
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

5.  Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.

Authors:  Heiko Krude; Barbara Schütz; Heike Biebermann; Arpad von Moers; Dirk Schnabel; Heidi Neitzel; Holger Tönnies; Dagmar Weise; Antony Lafferty; Siegfried Schwarz; Mario DeFelice; Andreas von Deimling; Frank van Landeghem; Roberto DiLauro; Annette Grüters
Journal:  J Clin Invest       Date:  2002-02       Impact factor: 14.808

6.  Mutations in TITF-1 are associated with benign hereditary chorea.

Authors:  Guido J Breedveld; Jeroen W F van Dongen; Cesare Danesino; Andrea Guala; Alan K Percy; Leon S Dure; Peter Harper; Lazarus P Lazarou; Herma van der Linde; Marijke Joosse; Annette Grüters; Marcy E MacDonald; Bert B A de Vries; Willem Frans M Arts; Ben A Oostra; Heiko Krude; Peter Heutink
Journal:  Hum Mol Genet       Date:  2002-04-15       Impact factor: 6.150

7.  Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.

Authors:  Friedrich Asmus; Anita Devlin; Marita Munz; Alexander Zimprich; Thomas Gasser; Patrick F Chinnery
Journal:  Mov Disord       Date:  2007-10-31       Impact factor: 10.338

8.  Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease.

Authors: 
Journal:  Cell       Date:  2015-07-30       Impact factor: 41.582

9.  Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.

Authors:  Ying-Zhang Chen; Jennifer R Friedman; Dong-Hui Chen; Guy C-K Chan; Cinnamon S Bloss; Fuki M Hisama; Sarah E Topol; Andrew R Carson; Phillip H Pham; Emily S Bonkowski; Erick R Scott; Janel K Lee; Guangfa Zhang; Glenn Oliveira; Jian Xu; Ashley A Scott-Van Zeeland; Qi Chen; Samuel Levy; Eric J Topol; Daniel Storm; Phillip D Swanson; Thomas D Bird; Nicholas J Schork; Wendy H Raskind; Ali Torkamani
Journal:  Ann Neurol       Date:  2014-03-13       Impact factor: 10.422

10.  Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.

Authors:  Ricardo Mouro Pinto; Ella Dragileva; Andrew Kirby; Alejandro Lloret; Edith Lopez; Jason St Claire; Gagan B Panigrahi; Caixia Hou; Kim Holloway; Tammy Gillis; Jolene R Guide; Paula E Cohen; Guo-Min Li; Christopher E Pearson; Mark J Daly; Vanessa C Wheeler
Journal:  PLoS Genet       Date:  2013-10-31       Impact factor: 5.917

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  8 in total

1.  Will New Genetic Techniques Like Exome Sequencing and Others Obviate the Need for Clinical Expertise? Yes.

Authors:  Vincenzo Bonifati
Journal:  Mov Disord Clin Pract       Date:  2016-10-17

Review 2.  Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for?

Authors:  Alessio Di Fonzo; Edoardo Monfrini; Roberto Erro
Journal:  Curr Neurol Neurosci Rep       Date:  2018-05-23       Impact factor: 5.081

Review 3.  Challenges in Clinicogenetic Correlations: One Gene - Many Phenotypes.

Authors:  Francesca Magrinelli; Bettina Balint; Kailash P Bhatia
Journal:  Mov Disord Clin Pract       Date:  2021-03-02

Review 4.  Challenges in Clinicogenetic Correlations: One Phenotype - Many Genes.

Authors:  Rahul Gannamani; Sterre van der Veen; Martje van Egmond; Tom J de Koning; Marina A J Tijssen
Journal:  Mov Disord Clin Pract       Date:  2021-03-02

5.  Novel Mutation in the TSFM Gene Causes an Early-Onset Complex Chorea without Basal Ganglia Lesions.

Authors:  Anne K van Riesen; Saskia Biskup; Andrea A Kühn; Angela M Kaindl; Christoph van Riesen
Journal:  Mov Disord Clin Pract       Date:  2021-02-05

6.  ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.

Authors:  Miryam Carecchio; Niccolò E Mencacci; Alessandro Iodice; Roser Pons; Celeste Panteghini; Giovanna Zorzi; Federica Zibordi; Anastasios Bonakis; Argyris Dinopoulos; Joseph Jankovic; Leonidas Stefanis; Kailash P Bhatia; Valentina Monti; Lea R'Bibo; Liana Veneziano; Barbara Garavaglia; Carlo Fusco; Nicholas Wood; Maria Stamelou; Nardo Nardocci
Journal:  Parkinsonism Relat Disord       Date:  2017-05-10       Impact factor: 4.891

7.  A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.

Authors:  Vincenzo Salpietro; Belen Perez-Dueñas; Kosuke Nakashima; Victoria San Antonio-Arce; Andreea Manole; Stephanie Efthymiou; Jana Vandrovcova; Conceicao Bettencourt; Niccolò E Mencacci; Christine Klein; Michy P Kelly; Ceri H Davies; Haruhide Kimura; Alfons Macaya; Henry Houlden
Journal:  Mov Disord       Date:  2018-02-02       Impact factor: 10.338

Review 8.  Novel Imaging Biomarkers for Huntington's Disease and Other Hereditary Choreas.

Authors:  Patrik Fazio; Martin Paucar; Per Svenningsson; Andrea Varrone
Journal:  Curr Neurol Neurosci Rep       Date:  2018-10-05       Impact factor: 5.081

  8 in total

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