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患有遗传性原发性高乳糜微粒血症的猫的周围神经病变

Peripheral neuropathy in cats with inherited primary hyperchylomicronaemia.

作者信息

Jones B R, Johnstone A C, Cahill J I, Hancock W S

出版信息

Vet Rec. 1986 Sep 13;119(11):268-72. doi: 10.1136/vr.119.11.268.

DOI:10.1136/vr.119.11.268
PMID:3022456
Abstract

Primary hyperlipoproteinaemia (hyperchylomicronaemia) with a slight increase in very low density lipoprotein) is described in 20 cats. Fasting hyperlipaemia, lipaemia retinalis and peripheral neuropathies were the most frequently detected clinical signs. The disease is thought to be inherited as an autosomal recessive trait but the exact mode of inheritance has not been determined. Affected cats showed reduced lipoprotein lipase activity measured after heparin activation compared with the response in normal cats. Plasma triglyceride and cholesterol were increased in all the cats with the major proportion of triglyceride and cholesterol being present in chylomicrons. The peripheral nerve lesions were caused by compression of nerves by lipid granulomata. It is probable that the lipid granulomata result from trauma because the nerves most often affected were at sites like the spinal foraminae where they were susceptible to trauma.

摘要

在20只猫中发现了原发性高脂蛋白血症(高乳糜微粒血症),伴有极低密度脂蛋白略有升高。空腹高脂血症、视网膜脂血症和周围神经病变是最常检测到的临床症状。该病被认为是作为常染色体隐性性状遗传,但确切的遗传模式尚未确定。与正常猫相比,受影响的猫在肝素激活后测得的脂蛋白脂肪酶活性降低。所有猫的血浆甘油三酯和胆固醇均升高,其中大部分甘油三酯和胆固醇存在于乳糜微粒中。周围神经病变是由脂质肉芽肿压迫神经所致。脂质肉芽肿很可能是由创伤引起的,因为最常受影响的神经位于脊髓孔等易受创伤的部位。

相似文献

1
Peripheral neuropathy in cats with inherited primary hyperchylomicronaemia.患有遗传性原发性高乳糜微粒血症的猫的周围神经病变
Vet Rec. 1986 Sep 13;119(11):268-72. doi: 10.1136/vr.119.11.268.
2
Occurrence of idiopathic, familial hyperchylomicronaemia in a cat.一只猫出现特发性、家族性高乳糜微粒血症。
Vet Rec. 1983 Jun 4;112(23):543-7. doi: 10.1136/vr.112.23.543.
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The pathology of an inherited hyperlipoproteinaemia of cats.猫遗传性高脂蛋白血症的病理学
J Comp Pathol. 1990 Feb;102(2):125-37. doi: 10.1016/s0021-9975(08)80118-1.
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The ultrastructural pathology of five lipoprotein lipase-deficient cats.五只脂蛋白脂肪酶缺乏猫的超微结构病理学
J Comp Pathol. 1989 Oct;101(3):251-62. doi: 10.1016/0021-9975(89)90034-0.
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Chylomicron and very-low-density lipoprotein levels in type I hyperlipoproteinaemia. The role of the liver in determining biochemical phenotype.I型高脂蛋白血症中乳糜微粒和极低密度脂蛋白水平。肝脏在决定生化表型中的作用。
S Afr Med J. 1982 Feb 20;61(8):266-72.
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Why very low density lipoprotein levels are normal in familial hyperchylomicronaemia.为什么家族性高乳糜微粒血症患者的极低密度脂蛋白水平正常。
Atherosclerosis. 1979 Sep;34(1):83-6. doi: 10.1016/0021-9150(79)90109-6.
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[Pathologic decrease in lipoprotein lipase activity in relation to the development of hyperlipemias and their significance for coronary heart disease].[脂蛋白脂肪酶活性病理性降低与高脂血症发生发展的关系及其对冠心病的意义]
Wien Klin Wochenschr Suppl. 1986;167:1-16.
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Primary type I hyperlipoproteinaemia--a metabolic and family study.原发性I型高脂蛋白血症——一项代谢与家族研究。
Aust N Z J Med. 1979 Dec;9(6):688-93. doi: 10.1111/j.1445-5994.1979.tb04201.x.
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Lipaemia retinalis in a 29-day-old infant with type 1 hyperlipoproteinaemia.一名患有1型高脂蛋白血症的29日龄婴儿出现视网膜脂血症。
Br J Ophthalmol. 1985 Apr;69(4):280-2. doi: 10.1136/bjo.69.4.280.
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Pathogenesis of type I hyperlipoproteinemia.
Monogr Atheroscler. 1986;14:135-9.

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