Oromandibular Dystonia: Clinical and Demographic Data from Eight-Two Patients.

IF 2.5 Q2 CLINICAL NEUROLOGY
Mehmet Balal, Meltem Demirkiran
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Abstract

Objective: This study aimed to determine the demographic and clinical characteristics of patients with oromandibular dystonia (OMD).

Background: Dystonia is a movement disorder characterized by sustained involuntary muscle contractions that often cause abnormal postures. OMD is a rare focal dystonia that affects the tongue, jaw, and mouth. OMD, which is a rare public health problem, is often recognized as psychogenic and there are delays in its diagnosis and treatment.

Methods: Patients with OMD, both isolated and combined, followed at our Movement Disorders Outpatient Clinic between 2004 and 2021 were enrolled in this study. Age, sex, age at onset, and disease duration were recorded. The type of OMD, affected muscles, etiologies of accompanying neurological disorders, and treatment were noted.

Results: A total of 82 patients (44 women, 38 men) were included in this study. Among these, 39 patients had isolated OMD, and 43 patients had either segmental or generalized dystonia. Seven patients reported a family history of dystonia. Only nine patients reported a sensory trick. The average disease duration was 6.01 ± 3.73 (range, 1-29) years, and the average age at onset was 43.34 ± 18.24 (range, 1-78) years. The disease etiology was unknown (idiopathic) in most patients. Fifteen patients reported task-specific dystonia. The most common type of dystonia was jaw-opening dystonia.

Conclusion: OMD is focal dystonia that significantly affects the quality of life. This study adds more data to the literature by defining the clinical features of this rare disorder and draws attention to this neglected type of dystonia.

口腔下颌肌张力障碍:来自82例患者的临床和人口统计学数据。
目的:本研究旨在确定口腔下颌肌张力障碍(OMD)患者的人口学和临床特征。背景:肌张力障碍是一种运动障碍,其特征是持续的不随意肌收缩,经常导致异常的姿势。OMD是一种罕见的局灶性肌张力障碍,影响舌、颌和口腔。强迫症是一种罕见的公共卫生问题,通常被认为是心因性的,在诊断和治疗方面存在延误。方法:2004年至2021年间在我们的运动障碍门诊诊所随访的OMD患者,包括孤立的和合并的。记录患者的年龄、性别、发病年龄和病程。记录了OMD的类型、受影响的肌肉、伴随神经系统疾病的病因和治疗方法。结果:本研究共纳入82例患者,其中女性44例,男性38例。其中39例为孤立性肌张力障碍,43例为节段性或全身性肌张力障碍。7例患者报告有肌张力障碍家族史。只有9名患者报告了感觉上的欺骗。平均病程6.01±3.73(范围,1 ~ 29)年,平均发病年龄43.34±18.24(范围,1 ~ 78)岁。大多数患者病因不明(特发性)。15名患者报告了任务特异性肌张力障碍。最常见的肌张力障碍类型是张口肌张力障碍。结论:OMD是局灶性肌张力障碍,显著影响生活质量。本研究通过定义这种罕见疾病的临床特征,为文献增加了更多的数据,并引起了对这种被忽视的肌张力障碍类型的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
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