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DYT6 型肌张力障碍:突变筛查、表型及脑深部电刺激反应。

DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.

机构信息

Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Mov Disord. 2010 Oct 30;25(14):2420-7. doi: 10.1002/mds.23285.

Abstract

Mutations in THAP1, a gene encoding a nuclear pro-apoptotic protein, have been associated with DYT6 dystonia. First reports on the phenotype of DYT6 dystonia show an early onset dystonia with predominant cranio-cervical and laryngeal involvement. Here we assessed the frequency and phenotype of THAP1 mutation carriers in a large Dutch cohort of adult-onset (≥26 years) dystonia (n = 388) and early-onset dystonia (n = 67) patients. We describe the phenotype of DYT6 dystonia patients and their response on GPi DBS. Overall, 3 nonsynonymous heterozygous mutations were detected in the early-onset group (4.5%). Two DYT6 families were identified, showing a heterozygous phenotype. All patients had segmental or generalized dystonia, often associated with profound oromandibular and laryngeal involvement. No nonsynonymous mutations were found in patients with adult-onset focal dystonia. Rare synonymous variants were identified in conserved regions of THAP1, two in the adult-onset cervical dystonia group and one in the control group. Four DYT6 dystonia patients were treated with GPi DBS with moderate to good response on motor function but marginal benefit on speech.

摘要

THAP1 基因突变与 DYT6 型肌张力障碍有关,该基因编码一种核促凋亡蛋白。最初关于 DYT6 型肌张力障碍表型的报告显示,早发性肌张力障碍以颅颈和喉受累为主。在此,我们在一个由成年起病(≥26 岁)(n=388)和早发性(n=67)肌张力障碍患者组成的大型荷兰队列中评估了 THAP1 突变携带者的频率和表型。我们描述了 DYT6 型肌张力障碍患者的表型及其对 GPi-DBS 的反应。总的来说,在早发性组(4.5%)检测到 3 个非同义杂合突变。确定了两个 DYT6 家系,表现为杂合表型。所有患者均有节段性或全身性肌张力障碍,常伴有严重的口颌和喉受累。在成年起病的局灶性肌张力障碍患者中未发现非同义突变。在 THAP1 的保守区域发现了罕见的同义变体,其中两个在成年起病的颈肌张力障碍组中发现,一个在对照组中发现。4 名 DYT6 型肌张力障碍患者接受了 GPi-DBS 治疗,运动功能有中度至良好的反应,但对言语的获益不大。

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