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兰开夏赫勒犬的柯利眼异常。

Collie eye anomaly in the Lancashire heeler.

作者信息

Bedford P G

机构信息

Department of Small Animal Medicine and Surgery, Royal Veterinary College, Hatfield, Hertfordshire.

出版信息

Vet Rec. 1998 Sep 26;143(13):354-6. doi: 10.1136/vr.143.13.354.

DOI:10.1136/vr.143.13.354
PMID:9800301
Abstract

An ocular disease ophthalmoscopically identical to collie eye anomaly (CEA) is described in the Lancashire heeler breed of terrier. Survey work completed in 1996 demonstrated a significant incidence of 13.7 per cent. The clinical findings together with initial pedigree analysis support the accepted view that, in the traditionally affected breeds, CEA is a true pleiomorph which segregates as a recessive Mendelian trait. Alternative hypothesis speculates that the several lesions ascribed to CEA may occur as separate congenital disease entities, each with its own mode of inheritance. However, the combination of bilateral chloroidal hypoplasia, papillary or peripapillary coloboma and neuroretinal non-attachment in a non-collie breed tends to confirm that these three lesions are indeed individual parts of the one disease. The established appearance of CEA outwith the collie breeds dictates that the nomenclature for this disease is now somewhat inappropriate and that an alternative name should be considered. It is suggested that the term 'congenital posterior segment anomaly' could be adopted.

摘要

在兰开夏赫勒梗犬品种中描述了一种在检眼镜下与柯利犬眼异常(CEA)相同的眼病。1996年完成的调查工作显示其发病率高达13.7%,相当显著。临床发现以及初步的系谱分析支持了一种公认的观点,即在传统上受影响的品种中,CEA是一种真正的多形性疾病,以隐性孟德尔性状进行分离。另一种假说是,归因于CEA的几种病变可能作为单独的先天性疾病实体出现,每种都有其自己的遗传方式。然而,在一个非柯利犬品种中出现双侧脉络膜发育不全、视乳头或视乳头周围缺损以及神经视网膜分离,这倾向于证实这三种病变确实是同一种疾病的不同部分。在柯利犬品种之外出现的CEA的既定表现表明,这种疾病的命名现在有点不合适,应该考虑一个替代名称。建议采用“先天性后段异常”这一术语。

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