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患有阵发性不自主运动的边境梗犬的临床特征

Clinical Features in Border Terrier Dogs with Paroxysmal Involuntary Movements.

作者信息

Marioni-Henry Katia, Rusbridge Clare, Volk Holger A

机构信息

Royal (Dick) School of Veterinary Studies Hospital for Small Animals, Veterinary Center The University of Edinburgh Roslin United Kingdom.

Fitzpatrick Referrals Godalming United Kingdom.

出版信息

Mov Disord Clin Pract. 2015 Nov 23;3(1):73-79. doi: 10.1002/mdc3.12232. eCollection 2016 Jan-Feb.

DOI:10.1002/mdc3.12232
PMID:30713898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6353441/
Abstract

BACKGROUND

There have been anecdotal reports of episodic involuntary movements in the Border Terrier dog breed for over a decade. Recently, it has been hypothesized that this condition may be a form of paroxysmal dystonic choreoathetosis. The aim of this study was to characterize the phenomenology and clinical course of this condition and compare it to known human movement disorders.

METHODS

Data were collected retrospectively from clinical cases treated by veterinary neurologists and additional information was collected prospectively with an ad-hoc online survey directed to owners of affected dogs.

RESULTS

The episodes are characterized by generalized dystonia, tremors, titubation, and, in some cases, autonomic signs, such as salivation and vomiting. The median age at onset of the episodes was 3 years and the interval between clusters of episodes could last several months. Most of the episodes occurred from rest, and 67% of the owners reported that the episodes were associated with a trigger, most often excitement. Some owners reported an improvement after changing their dog's diet. We hypothesize that the Border Terrier attacks represent a form of paroxysmal nonkinesigenic dyskinesia.

CONCLUSIONS

The finding of a dystonia phenotype within an inbred population suggests a genetic predisposition, and elucidating the genetic cause could facilitate improved understanding of dystonia. This genetic predisposition and the effect of treatment with anticonvulsant drugs and dietary changes on the severity of the paroxysms warrant further investigation on this condition.

摘要

背景

十多年来,一直有关于边境梗犬品种出现发作性不自主运动的轶事报道。最近,有人推测这种情况可能是阵发性肌张力障碍性舞蹈手足徐动症的一种形式。本研究的目的是描述这种情况的现象学和临床过程,并将其与已知的人类运动障碍进行比较。

方法

回顾性收集兽医神经科医生治疗的临床病例数据,并通过针对患病犬只主人的临时在线调查前瞻性收集额外信息。

结果

发作的特征为全身性肌张力障碍、震颤、点头运动,在某些情况下还伴有自主神经症状,如流涎和呕吐。发作的中位发病年龄为3岁,发作群之间的间隔可持续数月。大多数发作发生于休息时,67%的主人报告发作与触发因素有关,最常见的是兴奋。一些主人报告在改变犬只饮食后病情有所改善。我们推测边境梗犬的发作代表一种阵发性非运动诱发性运动障碍。

结论

在一个近亲繁殖群体中发现肌张力障碍表型提示存在遗传易感性,阐明遗传原因有助于更好地理解肌张力障碍。这种遗传易感性以及抗惊厥药物治疗和饮食改变对发作严重程度的影响值得对这种情况进行进一步研究。