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巴吉度猎犬的一种遗传性血小板功能缺陷。

An inherited platelet function defect in Basset hounds.

作者信息

Johnstone I B, Lotz F

出版信息

Can Vet J. 1979 Aug;20(8):211-5.

PMID:509382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1789573/
Abstract

An inherited platelet function defect occurring in a family of basset hounds has been described. The trait is transmitted as an autosomal characteristic and appears to be expressed clinically only in the homozygous state. The characteristics of this platelet defect include:1) marked bleeding tendencies and prolonged skin bleeding times in either male or female dogs.2) normal blood coagulation mechanism.3) adequate numbers of circulating platelets which appear morphologically normal by light microscopy.4) normal whole blood clot retraction.5) deficient in vivo platelet consumption and in vitro platelet retention in glass bead columns.6) defective ADP-induced platelet aggregation in homozygotes, apparently normal ADP response in heterozygotes, and defective collagen-induced platelet aggregation in both.

摘要

已描述了在一组巴吉度猎犬家族中出现的一种遗传性血小板功能缺陷。该性状作为常染色体特征进行传递,并且似乎仅在纯合状态下才在临床上表现出来。这种血小板缺陷的特征包括:1)雄性或雌性犬均有明显的出血倾向和延长的皮肤出血时间。2)正常的血液凝固机制。3)循环血小板数量充足,通过光学显微镜观察形态正常。4)全血凝块回缩正常。5)体内血小板消耗不足以及在玻璃珠柱中体外血小板滞留不足。6)纯合子中ADP诱导的血小板聚集缺陷,杂合子中ADP反应明显正常,两者中胶原蛋白诱导的血小板聚集均有缺陷。

相似文献

1
An inherited platelet function defect in Basset hounds.巴吉度猎犬的一种遗传性血小板功能缺陷。
Can Vet J. 1979 Aug;20(8):211-5.
2
Identification of an intrinsic platelet function defect in Spitz dogs.斯皮茨犬内在血小板功能缺陷的鉴定。
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Two-dimensional electrophoretic studies of platelets from dogs affected with basset hound hereditary thrombopathy: a thrombasthenia-like aggregation defect.患有巴吉度猎犬遗传性血栓形成病(一种类似血小板无力症的聚集缺陷)的犬类血小板的二维电泳研究
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Defective contact activation of platelets from dogs with basset hound hereditary thrombopathy.患有巴吉度猎犬遗传性血栓形成病的犬类血小板接触激活缺陷。
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Hereditary canine thrombopathia.遗传性犬类血栓形成异常
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Potential large animal models for gene therapy of human genetic diseases of immune and blood cell systems.用于人类免疫和血细胞系统遗传疾病基因治疗的潜在大型动物模型。
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本文引用的文献

1
THE AGGREGATION OF BLOOD PLATELETS.血小板的聚集
J Physiol. 1963 Aug;168(1):178-95. doi: 10.1113/jphysiol.1963.sp007185.
2
Familial canine thrombocytopathy.家族性犬血小板病
Thromb Diath Haemorrh Suppl. 1967;26:241-8.
3
Canine von Willebrand's disease.犬血管性血友病
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Decreased adhesion of platelets to subendothelium in von Willebrand's disease.血管性血友病中血小板与内皮下组织的黏附性降低。
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5
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.
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A standardized test of platelet adhesiveness.一项血小板黏附性的标准化测试。
Am J Clin Pathol. 1972 Oct;58(4):422-7. doi: 10.1093/ajcp/58.5.422.
7
Suspected thrombasthenia in a shetland sheepdog.一只设得兰牧羊犬疑似血小板无力症。
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8
Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.血管性血友病中瑞斯托霉素诱导的血小板聚集缺陷及其通过因子VIII的纠正。
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Willebrand factor and ristocetin. I. Mechanism of rustocetin-induced platelet aggregation.血管性血友病因子与瑞斯托霉素。I. 瑞斯托霉素诱导血小板聚集的机制。
Br J Haematol. 1974 Dec;28(4):561-78. doi: 10.1111/j.1365-2141.1974.tb06675.x.
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Further studies of canine von Willebrand's disease.犬类血管性血友病的进一步研究。
Blood. 1975 Feb;45(2):221-30.