Literature DB >> 25620691

Diagnosis and treatment of chorea syndromes.

Andreas Hermann1, Ruth H Walker.   

Abstract

Chorea is a common movement disorder which can be caused by a large variety of diseases including neurodegenerative diseases, metabolic diseases, and autoimmune diseases, or can be secondary to structural changes. The basal ganglia seem to be mainly involved in the pathophysiology indicating the vulnerability of this region. The diagnosis can be challenging, especially if chorea occurs during the treatment of neuropsychiatric conditions, and in these cases, it is difficult to distinguish between medication side effects (i.e., tardive dyskinesia) and the development of a neurodegenerative disease. Most therapeutic approaches are predominantly symptomatic, with a focus on multidisciplinary care for many patients. Nevertheless, some underlying diseases can be successfully treated and must not be missed. In this review, we summarize recent new developments in the differential diagnosis of chorea syndromes and suggest a pathway for a successful diagnosis of chorea in infancy, childhood, and adulthood for daily practice.

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Year:  2015        PMID: 25620691     DOI: 10.1007/s11910-014-0514-0

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  116 in total

1.  Slow evolution of cerebellar degeneration and chorea in a man with anti-Yo antibodies.

Authors:  P Krolak-Salmon; G Androdias; D Meyronet; M Aguera; J Honnorat; A Vighetto
Journal:  Eur J Neurol       Date:  2006-03       Impact factor: 6.089

2.  Schizophrenia in a patient with spinocerebellar ataxia 2: coincidence of two disorders or a neurodegenerative disease presenting with psychosis?

Authors:  Matthew Rottnek; Silvana Riggio; William Byne; Mary Sano; Russell L Margolis; Ruth H Walker
Journal:  Am J Psychiatry       Date:  2008-08       Impact factor: 18.112

3.  Adult-onset chorea and mitochondrial cytopathy.

Authors:  Morgane Caer; Karine Viala; Richard Levy; Thierry Maisonobe; Florence Chochon; Agnès Lombès; Yves Agid
Journal:  Mov Disord       Date:  2005-04       Impact factor: 10.338

4.  The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.

Authors:  D H Geschwind; S Perlman; C P Figueroa; L J Treiman; S M Pulst
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

5.  Primary Sjogren's syndrome presenting as a generalized chorea.

Authors:  P Venegas Fanchke; M Sinning; M Miranda
Journal:  Parkinsonism Relat Disord       Date:  2005-05       Impact factor: 4.891

Review 6.  Differential diagnosis of chorea.

Authors:  Ruth H Walker
Journal:  Curr Neurol Neurosci Rep       Date:  2011-08       Impact factor: 5.081

7.  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

8.  Benign hereditary chorea: clinical, neuroimaging, and genetic findings.

Authors:  Muhammad Mahajnah; Dov Inbar; Adam Steinmetz; Peter Heutink; G J Breedveld; Rachel Straussberg
Journal:  J Child Neurol       Date:  2007-10       Impact factor: 1.987

Review 9.  Therapeutic interventions for disease progression in Huntington's disease.

Authors:  Tiago Mestre; Joaquim Ferreira; Miguel M Coelho; Mário Rosa; Cristina Sampaio
Journal:  Cochrane Database Syst Rev       Date:  2009-07-08

10.  Chorea as the presenting feature of neurosyphilis.

Authors:  Serkan Ozben; Canan Erol; Feriha Ozer; Raziye Tiras
Journal:  Neurol India       Date:  2009 May-Jun       Impact factor: 2.117

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  23 in total

1.  Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility.

Authors:  Wondwossen M Yeshaw; Marianne van der Zwaag; Francesco Pinto; Liza L Lahaye; Anita Ie Faber; Rubén Gómez-Sánchez; Amalia M Dolga; Conor Poland; Anthony P Monaco; Sven Cd van IJzendoorn; Nicola A Grzeschik; Antonio Velayos-Baeza; Ody Cm Sibon
Journal:  Elife       Date:  2019-02-11       Impact factor: 8.140

Review 2.  Recent advances in genetics of chorea.

Authors:  Niccolò E Mencacci; Miryam Carecchio
Journal:  Curr Opin Neurol       Date:  2016-08       Impact factor: 5.710

Review 3.  An Update on the Treatment of Chorea.

Authors:  Erin Feinstein; Ruth Walker
Journal:  Curr Treat Options Neurol       Date:  2018-09-25       Impact factor: 3.598

Review 4.  Neuroacanthocytosis: Observations, Theories and Perspectives on the Origin and Significance of Acanthocytes.

Authors:  Merel J W Adjobo-Hermans; Judith C A Cluitmans; Giel J C G M Bosman
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-08-25

5.  De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions.

Authors:  Niccolò E Mencacci; Erik-Jan Kamsteeg; Kosuke Nakashima; Lea R'Bibo; David S Lynch; Bettina Balint; Michèl A A P Willemsen; Matthew E Adams; Sarah Wiethoff; Kazunori Suzuki; Ceri H Davies; Joanne Ng; Esther Meyer; Liana Veneziano; Paola Giunti; Deborah Hughes; F Lucy Raymond; Miryam Carecchio; Giovanna Zorzi; Nardo Nardocci; Chiara Barzaghi; Barbara Garavaglia; Vincenzo Salpietro; John Hardy; Alan M Pittman; Henry Houlden; Manju A Kurian; Haruhide Kimura; Lisenka E L M Vissers; Nicholas W Wood; Kailash P Bhatia
Journal:  Am J Hum Genet       Date:  2016-04-07       Impact factor: 11.025

Review 6.  Management of Neuroacanthocytosis Syndromes.

Authors:  Ruth H Walker
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-10-19

Review 7.  The non-Huntington disease choreas: Five new things.

Authors:  Ruth H Walker
Journal:  Neurol Clin Pract       Date:  2016-04

8.  Targeting Lyn Kinase in Chorea-Acanthocytosis: A Translational Treatment Approach in a Rare Disease.

Authors:  Kevin Peikert; Hannes Glaß; Enrica Federti; Alessandro Matte; Lisann Pelzl; Katja Akgün; Tjalf Ziemssen; Rainer Ordemann; Florian Lang; The Network For Translational Research For Neuroacanthocytosis Patients; Lucia De Franceschi; Andreas Hermann
Journal:  J Pers Med       Date:  2021-05-10

9.  Deleterious mutation in GPR88 is associated with chorea, speech delay, and learning disabilities.

Authors:  Fadi Alkufri; Avraham Shaag; Bassam Abu-Libdeh; Orly Elpeleg
Journal:  Neurol Genet       Date:  2016-03-09

10.  Chorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degeneration.

Authors:  Ito Kawakami; Zen Kobayashi; Tetsuaki Arai; Osamu Yokota; Takashi Nonaka; Naoya Aoki; Kazuhiro Niizato; Kenichi Oshima; Shinji Higashi; Omi Katsuse; Masato Hosokawa; Masato Hasegawa; Haruhiko Akiyama
Journal:  Acta Neuropathol Commun       Date:  2016-04-04       Impact factor: 7.801

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