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Characterization and Mode of Inheritance of a Paroxysmal Dyskinesia in Chinook Dogs

机译:奇努克犬阵发性运动障碍的特征和遗传模式。

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Background: Paroxysmal dyskinesias are episodes of abnormal, involuntary movement or muscle tone, distinguished from seizures by the character of the episode and lack of seizure activity on ictal EEG.Hypothesis: Paroxysmal dyskinesia is an inherited, autosomal recessive disorder in Chinook dogs.Animals: Families of Chinook dogs with paroxysmal dyskinesia.Methods: Pedigrees and medical histories were reviewed for 299 Chinook dogs. A family of 51 dogs was used for analysis. Episodes were classified as seizures, paroxysmal dyskinesia, or unknown, and segregation analysis was performed.Results: Paroxysmal dyskinesia was identified in 16 of 51 dogs and characterized by an inability to stand or ambulate, head tremors, and involuntary flexion of 1 or multiple limbs, without autonomic signs or loss of consciousness. Episode duration varied from minutes to an hour. Inter-ictal EEGs recorded on 2 dogs with dyskinesia were normal. Three dogs with dyskinesia also had generalized tonic-clonic seizures. One of 51 dogs had episodes of undetermined type. Phenotype was unknown for 6 of 51 dogs, and 28 dogs were unaffected. Segregation was consistent with an autosomal recessive trait.Conclusions and Clinical Importance: This movement disorder is prevalent in the Chinook breed, and consistent with a partially penetrant autosomal recessive or polygenic trait. Insufficient evidence exists for definitive localization; episodes may be of basal nuclear origin, but atypical seizures and muscle membrane disorders remain possible etiologies. The generalized seizures may be a variant phenotype of the same mutation that results in dyskinesia, or the 2 syndromes may be independent.
机译:背景:阵发性运动障碍是发作异常,不自主运动或肌肉紧张的发作,通过发作的特征和发作性发作而对发作性癫痫发作脑电图缺乏癫痫发作活动有所区别。假说:阵发性运动障碍是支努干犬中一种遗传性常染色体隐性遗传疾病。方法:对299只奇努克犬的谱系和病史进行回顾。使用51只狗的家庭进行分析。将发作分为癫痫发作,阵发性运动障碍或未知发作,并进行隔离分析。结果:在51只狗中有16只被识别出阵发性运动障碍,其特征是站立或行走不下,头部震颤以及1条或多条肢体不自主屈曲,没有自主神经体征或意识丧失。情节持续时间从几分钟到一个小时不等。在两只运动障碍犬中记录的发作间脑电图正常。三只运动障碍犬也普遍出现强直阵挛性癫痫发作。 51只狗中的一只患有不确定类型的发作。表型为51只狗中的6只未知,而28只狗未受影响。分离与常染色体隐性遗传特征一致。结论和临床意义:这种运动障碍在奇努克族中很普遍,并且与部分渗透的常染色体隐性遗传或多基因特征一致。现有的证据不足以进行确定的本地化;发作可能是基础核起源,但非典型性癫痫和肌膜疾病仍是可能的病因。全身性癫痫发作可能是导致运动障碍的同一突变的变异表型,或者这两种综合征可能是独立的。

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