Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/38221
Title: Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia
Authors: Silva-Junior, Francisco Pereira da
Santos, Camila Oliveira dos
Cesar Azevedo Silva, Sonia Maria [UNIFESP]
Barbosa, Egberto Reis
Borges, Vanderci [UNIFESP]
Ferraz, Henrique Ballalai [UNIFESP]
Papaterra Limongi, Joao Carlos
Guimaraes Rocha, Maria Sheila
Aguiar, Patricia de Carvalho [UNIFESP]
Universidade de São Paulo (USP)
Hosp Israelita Albert Einstein
Hosp Servidor Publ Estadual
Universidade Federal de São Paulo (UNIFESP)
Hosp Santa Marcelina
Keywords: Dystonia
THAP1
DYT6
TOR1A
Non-motor symptoms
Issue Date: 15-Sep-2014
Publisher: Elsevier B.V.
Citation: Journal of the Neurological Sciences. Amsterdam: Elsevier B.V., v. 344, n. 1-2, p. 190-192, 2014.
Abstract: THAP1 mutations are associated with idiopathic isolated dystonia in different ethnicities, but the importance of this gene as a cause of dystonia in the Brazilian population has not been determined. the aim of this study was to investigate the prevalence of THAP1 variants in Brazilian patients with idiopathic dystonia and to describe their clinical characteristics including non-motor symptoms. One hundred and ten unrelated patients with non-TOR1A (DYT1) idiopathic isolated dystonia and family members were evaluated and screened for genetic variants. Variants with a potential pathological role were observed in 9.0% of families studied, of which four were novel. the variants were identified in approximately 12% of patients with the age of onset below 40 years. in most of the patients, the onset of the disease was before early adulthood. the upper limb was the most common site of the onset, and approximately half of the patients had dysphonia. Pain, anxiety, and sleep-onset insomnia were the most prevalent non-motor symptoms, and their prevalence was not different from that observed in THAP1-negative patients. Therefore, THAP1 variants are an important cause of dystonia among individuals with an early-onset disease and a positive family history. the phenotypical heterogeneity among patients carrying similar variants shows that other factors may be modulating the disease. (C) 2014 Elsevier B.V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/38221
ISSN: 0022-510X
Other Identifiers: http://dx.doi.org/10.1016/j.jns.2014.06.012
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