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斯芬克斯猫发作性运动障碍的表型特征。

Phenotypic characterisation of paroxysmal dyskinesia in Sphynx cats.

机构信息

Dovecote Veterinary Hospital, Derby, UK.

Vet Oracle Teleradiology, Bedford, UK.

出版信息

J Feline Med Surg. 2022 Jun;24(6):500-505. doi: 10.1177/1098612X211032123. Epub 2021 Jul 27.

Abstract

OBJECTIVES

The aim of this study was to identify the phenotypic features of a paroxysmal dyskinesia observed in Sphynx cats.

METHODS

The owners of affected Sphynx cats were invited to provide video footage of abnormal episodes for review. Those that demonstrated episodes consistent with paroxysmal dyskinesia were then invited to complete an online questionnaire designed to allow further characterisation.

RESULTS

Ten Sphynx cats were included in the study. All affected cats were <4 years of age at the onset of the episodes (range 0.5-4.0). The episodes had a duration of <5 mins in 9/10 cats (range 0.5-10), while episode frequency was variable between and within individual cats. The episodes were characterised by impaired ambulation due to muscle hypertonicity, most commonly affecting the hips and pelvic limbs (9/10) and shoulders and thoracic limbs (8/10). The head and neck (6/10), tail (5/10), and back and abdomen (3/10) were also involved in some cats. Sudden movement, excitement and stress were identified as possible triggers for the episodes in three cats. Therapeutic intervention was not attempted in 7/10 cases, although two cats were reported to become free of the episodes while receiving acetazolamide. The two cats that were followed beyond 2 years from onset entered spontaneous remission. None of the owners believed that the abnormal episodes had affected the quality of life of their cat.

CONCLUSIONS AND RELEVANCE

The phenotype of paroxysmal dyskinesia in Sphynx cats presented in this study appears to share similarities with paroxysmal kinesigenic dyskinesia described in human classification systems. Some cats appear to achieve episode freedom spontaneously. Subsequent research should focus on evaluating response to treatment and determining an underlying genetic cause.

摘要

目的

本研究旨在确定斯芬克斯猫阵发性运动障碍的表型特征。

方法

邀请受影响的斯芬克斯猫的主人提供异常发作的视频片段进行审查。那些表现出与阵发性运动障碍一致的发作的猫随后被邀请完成一个在线问卷,以允许进一步的特征描述。

结果

本研究纳入了 10 只斯芬克斯猫。所有受影响的猫在发作时<4 岁(0.5-4.0 岁)。9/10 只猫的发作持续时间<5 分钟(0.5-10 分钟),而发作频率在个体猫之间和内部均有所不同。发作的特点是肌肉张力过高导致运动障碍,最常见于臀部和骨盆肢体(9/10)和肩部和胸部肢体(8/10)。头部和颈部(6/10)、尾巴(5/10)以及背部和腹部(3/10)也在一些猫中受累。3 只猫确定了发作的可能触发因素为突然运动、兴奋和应激。在 7/10 例中未尝试治疗干预,尽管有 2 只猫在接受乙酰唑胺治疗时发作停止。2 只在发病后 2 年以上随访的猫自发缓解。没有主人认为异常发作影响了猫的生活质量。

结论和相关性

本研究中斯芬克斯猫阵发性运动障碍的表型似乎与人类分类系统中描述的阵发性运动诱发性运动障碍相似。一些猫似乎自发地发作停止。后续研究应集中评估治疗反应和确定潜在的遗传原因。

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