New algorithm for the diagnosis of hereditary dystonia

Author:

Camargos Sarah1,Cardoso Francisco1

Affiliation:

1. Universidade Federal de Minas Gerais, Brazil

Abstract

Taking into account the crescent interest in the field of dystonia genetics, we have organized a didactic and fast algorithm to diagnose the main forms of hereditary dystonias. The key branch of this algorithm is pointed to dystonia classification in primary, plus, or paroxysmal. The specific characteristics of each syndrome will reveal the diagnosis.

Publisher

FapUNIFESP (SciELO)

Subject

Neurology,Neurology (clinical)

Reference21 articles.

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2. The diagnosis of dystonia;Geyer HL;Lancet Neurol,2006

3. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia;Bressman SB;Mov Disord,1994

4. Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites;Saunders-Pullman R;Am J Med Genet,2007

5. Evidence for locus heterogeneity in autosomal dominant torsion dystonia;Ahmad F;Genomics,1993

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Dystonias;CONTINUUM: Lifelong Learning in Neurology;2019-08

2. Treatable inherited rare movement disorders;Movement Disorders;2017-09-01

3. Understanding dystonia: diagnostic issues and how to overcome them;Arquivos de Neuro-Psiquiatria;2016-11

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