Literature DB >> 22622408

Phenotypic differences in Dyt1 between ethnic groups.

Woong-Woo Lee1, Tae-Beom Ahn, Sun Ju Chung, Beom Seok Jeon.   

Abstract

A DYT1 mutation is the most common genetic cause of early-onset primary torsion dystonia. Herein we present the phenotypes of 25 Korean dystonia patients with DYT1 mutations. We further compare the clinical features of the Asian patients with those of the Western DYT 1 mutation patients. In Korean patients, upper extremity was the most common site of symptom onset while there were a few patients with axial-onset dystonia. Generalized dystonia was the most common subtype followed by segmental dystonia. A few patients from the same families had their symptoms at the same age. The clinical features of Korean patients were similar to those of other Asian patients. The Asian patients were differentiated from Western patients by more frequent axial onset, no cranial involvement at onset, and more common segmental dystonia. The variable clinical manifestation in different ethnic groups may suggest that ethnicity is a significant modifier of DYT1 dystonia.

Entities:  

Mesh:

Year:  2012        PMID: 22622408     DOI: 10.1007/s11910-012-0285-4

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


  27 in total

1.  DYT1 mutation in Japanese patients with primary torsion dystonia.

Authors:  S Matsumoto; M Nishimura; R Kaji; T Sakamoto; T Mezaki; H Shimazu; N Murase; H Shibasaki
Journal:  Neuroreport       Date:  2001-03-26       Impact factor: 1.837

2.  DYT1 mutation in Korean primary dystonia patients.

Authors:  Joo-Hyuk Im; Tae-Beom Ahn; Ki Beom Kim; Sang-Bae Ko; Beom S Jeon
Journal:  Parkinsonism Relat Disord       Date:  2004-10       Impact factor: 4.891

3.  DYT1 mutation in primary torsion dystonia in a Serbian population.

Authors:  T Major; M Svetel; S Romac; V S Kostić
Journal:  J Neurol       Date:  2001-11       Impact factor: 4.849

4.  Embouchure dystonia--Portrait of a task-specific cranial dystonia.

Authors:  Steven J Frucht
Journal:  Mov Disord       Date:  2009-09-15       Impact factor: 10.338

5.  Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystonia.

Authors:  Mattia Gambarin; Enza Maria Valente; Paolo Liberini; Giuseppe Barrano; Alberto Bonizzato; Alessandro Padovani; Giuseppe Moretto; Mirta Fiorio; Bruno Dallapiccola; Nicola Smania; Antonio Fiaschi; Michele Tinazzi
Journal:  Mov Disord       Date:  2006-10       Impact factor: 10.338

6.  Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China.

Authors:  S-S Zhang; D-F Fang; X-H Hu; J-M Burgunder; X-P Chen; Y-W Zhang; H-F Shang
Journal:  Eur J Neurol       Date:  2010-01-26       Impact factor: 6.089

7.  GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.

Authors:  C Kamm; E Castelon-Konkiewitz; M Naumann; F Heinen; M Brack; A Nebe; A Ceballos-Baumann; T Gasser
Journal:  Mov Disord       Date:  1999-07       Impact factor: 10.338

8.  DYT1 mutation in French families with idiopathic torsion dystonia.

Authors:  A S Lebre; A Durr; P Jedynak; G Ponsot; M Vidailhet; Y Agid; A Brice
Journal:  Brain       Date:  1999-01       Impact factor: 13.501

9.  Frequency of DYT1 mutation in early onset primary dystonia in Italian patients.

Authors:  Giovanna Zorzi; Barbara Garavaglia; Federica Invernizzi; Floriano Girotti; Paola Soliveri; Massimo Zeviani; Lucia Angelini; Nardo Nardocci
Journal:  Mov Disord       Date:  2002-03       Impact factor: 10.338

Review 10.  Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature.

Authors:  Mark Edwards; Nicholas Wood; Kailash Bhatia
Journal:  Mov Disord       Date:  2003-06       Impact factor: 10.338

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  1 in total

Review 1.  Isolated dystonia: clinical and genetic updates.

Authors:  Aloysius Domingo; Rachita Yadav; Laurie J Ozelius
Journal:  J Neural Transm (Vienna)       Date:  2020-11-27       Impact factor: 3.575

  1 in total

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