The story of equine atypical myopathy: a review from the beginning to a possible end.

ISRN veterinary science Pub Date : 2012-11-14 Print Date: 2012-01-01 DOI:10.5402/2012/281018
Dominique-Marie Votion
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引用次数: 17

Abstract

Atypical myopathy (AM) is a frequently fatal seasonal pasture myopathy that emerges in Europe. Outbreaks are of an acute and unexpected nature and practitioners should be prepared to handle these critically ill patients. This review retraces the history of AM and describes results of epidemiological investigations that were conducted to raise hypotheses concerning the etiology of this devastating disease as well as to be able to suggest potential preventive measures. Also, clinical studies have contributed to a better definition and recognition of the syndrome, whereas elucidation of the pathological process, identified as a multiple acyl-CoA dehydrogenase deficiency (MADD), was a great step forward improving medical management of AM and guiding the search for the etiological agent towards toxins that reproduce the identified defect. Treatment plans can be extrapolated from the described clinical signs and metabolic problems, but they remain limited to supportive care until the causative agent has been identified with certainty. Since treatment is still unsuccessful in the majority of cases, the main emphasis is currently still on prevention. This paper aims at being a practical support for equine clinicians dealing with AM and is based on discussion and comparison of the currently available scientific data.

马非典型肌病的故事:从开始到可能结束的回顾。
非典型肌病(AM)是一种经常致命的季节性牧场肌病,出现在欧洲。疫情具有急性和意外的性质,从业人员应做好处理这些危重病人的准备。这篇综述回顾了AM的历史,并描述了流行病学调查的结果,这些调查的目的是提出关于这一毁灭性疾病的病因的假设,并能够提出潜在的预防措施。此外,临床研究有助于更好地定义和识别该综合征,而病理过程的阐明,被确定为多酰基辅酶a脱氢酶缺乏症(MADD),是向前迈进了一大步,改善了AM的医学管理,并指导寻找致病因子,使毒素复制所识别的缺陷。治疗方案可以从所描述的临床症状和代谢问题中推断出来,但在确定病原体之前,它们仍然局限于支持性护理。由于大多数病例的治疗仍然不成功,目前的主要重点仍然是预防。本文旨在成为马临床医生处理AM的实际支持,并基于对当前可用科学数据的讨论和比较。
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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