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三只同窝小猫的遗传性小脑变性

Hereditary cerebellar degeneration in three full sibling kittens.

作者信息

Willoughby K, Kelly D F

机构信息

Department of Veterinary Clinical Science and Animal Husbandry, University of Liverpool.

出版信息

Vet Rec. 2002 Sep 7;151(10):295-8. doi: 10.1136/vr.151.10.295.

Abstract

Two domestic shorthair littermate kittens had signs of cerebellar dysfunction, first observed between seven and eight weeks of age; a third littermate was unaffected. The signs were progressive and the more severely affected kitten was euthanased after six days. A postmortem examination revealed no gross lesions but the kitten had cerebellar cortical degeneration with extensive loss of Purkinje cells. The second kitten was euthanased at 10 months of age with similar, though more pronounced, changes. One of the two kittens in the next litter of the same parents had similar clinical signs and histopathological findings. The lesions in the cerebellum are interpreted as probably due to genetically determined abiotrophy. In addition, the two older kittens had medullary neuronal changes interpreted as probable neuraxonal dystrophy, and focal vacuolation of the neuropil in the medulla and cervical spinal cord.

摘要

两只家养短毛同窝小猫出现小脑功能障碍的症状,最早在7至8周龄时被观察到;第三只同窝小猫未受影响。症状呈进行性发展,病情较重的那只小猫在6天后实施了安乐死。尸检未发现明显病变,但这只小猫存在小脑皮质变性,浦肯野细胞大量丧失。第二只小猫在10月龄时因类似但更为明显的变化而实施安乐死。同一对父母的下一窝小猫中的两只也出现了类似的临床症状和组织病理学发现。小脑病变被认为可能是由基因决定的营养障碍所致。此外,两只较大的小猫存在延髓神经元变化,被认为可能是神经轴突营养不良,延髓和颈脊髓的神经纤维网有局灶性空泡形成。

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