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古代英国牧羊犬的小脑变性

Cerebellar degeneration in Old English Sheepdogs.

作者信息

Steinberg H S, Van Winkle T, Bell J S, de Lahunta A

机构信息

VCA Veterinary Referral Associates, Gaithersburg, MD 20878, USA.

出版信息

J Am Vet Med Assoc. 2000 Oct 15;217(8):1162-5. doi: 10.2460/javma.2000.217.1162.

Abstract

OBJECTIVE

To evaluate related and unrelated Old English Sheepdogs (OESD) by clinical examination, histologic evaluation, and pedigree analysis to determine whether cerebellar degeneration develops in this breed and whether there are genetic implications.

DESIGN

Case study and pedigree analysis.

ANIMALS

24 clinically normal or affected OESD; brain tissue specimens from 25 unaffected or affected OESD.

PROCEDURE

Twenty-four OESD that were chosen because of a family history of gait abnormalities were given physical and neurologic examinations to determine whether they had clinical signs of cerebellar degeneration. Tissue specimens from 25 brains of OESD were examined histologically. Nine OESD that were determined to have cerebellar degeneration histologically as well as 2 clinically affected littermates of the histologically confirmed affected OESD were included in the pedigree analysis. Standard statistical evaluation of pedigrees for hereditary conclusions was used.

RESULTS

Twelve of the 24 OESD evaluated by neurologic examination had a progressive gait abnormality. Clinical signs of cerebellar degeneration typically started later in life in OESD, compared with description for other dog breeds, and progressed ore slowly. Results of pedigree analysis revealed that 11 of 49 dogs were affected in 9 litters, providing an affected-to-total ratio of 22.49%.

CONCLUSIONS AND CLINICAL RELEVANCE

Results of our study indicate that a slowly progressing late-onset form of cerebellar degeneration develops in OESD, and the mode of inheritance is by an autosomal recessive gene.

摘要

目的

通过临床检查、组织学评估和系谱分析,对有亲缘关系和无亲缘关系的古代英国牧羊犬(OESD)进行评估,以确定该品种是否会发生小脑退化以及是否存在遗传影响。

设计

病例研究和系谱分析。

动物

24只临床正常或患病的OESD;25只未受影响或受影响的OESD的脑组织标本。

步骤

选取24只因步态异常家族史而被选中的OESD进行体格和神经学检查,以确定它们是否有小脑退化的临床症状。对25只OESD的脑组织标本进行组织学检查。将9只经组织学确定患有小脑退化的OESD以及2只经组织学确诊受影响的OESD的临床患病同窝仔犬纳入系谱分析。使用系谱的标准统计评估得出遗传结论。

结果

经神经学检查评估的24只OESD中有12只出现进行性步态异常。与其他犬种的描述相比,OESD中小脑退化的临床症状通常在生命后期出现,且进展较慢。系谱分析结果显示,49只犬中有11只在9窝中受影响,受影响与总数的比例为22.49%。

结论及临床意义

我们的研究结果表明,OESD会出现一种进展缓慢、发病较晚的小脑退化形式,遗传方式为常染色体隐性基因。

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