犬的遗传性婴儿扩张型心肌病:遗传、临床、生化和形态学的发现。

American Journal of Medical Genetics Pub Date : 2000-11-06
J Alroy, J E Rush, L Freeman, M S Amarendhra Kumar, A Karuri, K Chase, S Sarkar
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引用次数: 0

摘要

扩张型心肌病是一种以左心室扩张和收缩功能障碍为特征的致命疾病,在人类和其他哺乳动物中相对常见。特发性扩张型心肌病(IDCM)是一种病因不明的原发性心肌疾病,可能是一种家族性疾病。本报告描述犬常染色体隐性IDCM。它发生在葡萄牙水犬(PWD)幼崽,表现为急性,模糊的临床症状和猝死。受影响的幼犬在出现临床症状之前,可通过超声心动图证实其渐进式缩短。此外,这些幼崽在食用某些食物时血浆牛磺酸水平较低。受影响的幼犬左心室扩张,肌瘤外观改变,而免疫组织化学和生化研究表明,desmin(一种细胞骨架蛋白)增加。残疾患者IDCM的临床和形态学表现不同于成人IDCM。最后,一些幼犬在口服牛磺酸2个月后的临床和超声心动图表现是可逆的。这些结果表明,pwd患者的IDCM与低血浆牛磺酸水平相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inherited infantile dilated cardiomyopathy in dogs: genetic, clinical, biochemical, and morphologic findings.

Dilated cardiomyopathy, a lethal disease characterized by left ventricular dilation and systolic dysfunction, is relatively common in humans and other mammals. Idiopathic dilated cardiomyopathy (IDCM) is a primary myocardial disease of unknown cause and can be a familial disorder. This report describes autosomal recessive IDCM in dogs. It occurs in Portuguese Water Dog (PWD) pups and is manifested by acute, vague clinical signs and sudden death. Affected pups have progressive reduction of fractional shortening that can be demonstrated by echocardiography prior to the development of clinical signs. Furthermore, these pups have low plasma taurine levels when consuming certain diets. Affected pups had dilation of the left ventricle and alterations in the sarcomere appearance, while immunohistochemical and biochemical studies demonstrate an increase in desmin, a cytoskeleton protein. The clinical and morphologic findings of IDCM in PWDs are distinct from those reported in adult IDCM. Finally, the clinical and echocardiographic manifestations were reversible in some pups following oral taurine supplementation for 2 months. These results suggest that IDCM in PWDs is correlated with low plasma taurine levels.

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