...
首页> 外文期刊>Small animal medicine digest >Feline Mucopolysaccharidosis VII Due to (3-Glucuronidase Deficiency
【24h】

Feline Mucopolysaccharidosis VII Due to (3-Glucuronidase Deficiency

机译:由于(3-葡萄糖醛酸酶缺乏症)猫的粘多糖贮积症VII

获取原文
获取原文并翻译 | 示例

摘要

Mucopolysacchari-doses (MPS) are lysosomal storage disorders caused by the deficiency of a lysosomal hydrolase needed for mu-copolysacchatide degradation, To date, only MPS I and VI have been reported in cats. The first case of MPS VII in a cat was described. Domestic short-haired male cat, 12-14 weeks old, was seen for assessment of walking difficulty and an enlarged abdomen. Examination revealed coineal clouding, plump front paws with inside rotation, and mild skin thickening, especially over the paws, Mucopolysacchari-dosis was suspected. The result of a toluidine test for sulfated glycosaminogly-cans in the urine was positive Radiographic findings, excessive granulation of neutrophil granulocytes, and intense vacuolation of lymphocytes prompteda biochemical analysis, and beta-glucuronidase deficiency was found.
机译:粘多糖贮积症(MPS)是由粘多糖降解所需的溶酶体水解酶缺乏引起的溶酶体贮积病。迄今为止,在猫中仅报道了MPS I和VI。描述了猫中MPS VII的第一例。观察到12-14周龄的家养短毛公猫,以评估其行走困难和腹部扩大。检查发现前突浑浊,前爪饱满并向内旋转,皮肤轻度增厚,尤其是爪子上方,怀疑是粘多糖病。尿液中硫酸化糖胺糖罐头的甲苯胺检测结果为放射线阳性,嗜中性粒细胞粒化过多,淋巴细胞强烈空泡化,提示生化分析,发现β-葡糖醛酸糖苷酶缺乏症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号