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31只犬进行性视网膜萎缩的临床研究。

Clinical studies on progressive retinal atrophy in 31 dogs.

作者信息

Kelawala D N, Patil D B, Parikh P V, Sheth M J, Joshi C G, Reddy B

机构信息

Ph.D. Scholar in Veterinary Surgery and Radiology, Department of Veterinary Surgery and Radiology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand, Gujarat-388001, India.

Department of Veterinary Surgery and Radiology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand, Gujarat-388001, India.

出版信息

Iran J Vet Res. 2017 Spring;18(2):119-123.

PMID:28775752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5534255/
Abstract

During a 2-year period, 31 cases of a hereditary retinal degeneration in dogs bred in India were found mainly suspected for progressive retinal atrophy (PRA) with typical history of initial nyctalopia followed by hemeralopia. Out of 31 PRA suspected dogs, 8 dogs (26%) were from the age group of 1-5 years, 15 (48%) 6-10 years and the rest (26%) 11-15 years. The most predominant breed was Spitz (18 dogs, 58%). Detailed ophthalmologic examinations included Schirmer's tear test, fluorescein stain, applanation tonometry, slit lamp biomicroscopy and ocular ultrasound in appropriate cases. Ophthalmoscopic and fundoscopic changes included hyperreflectivity and discoloration of the tapetal area, marked attenuation of retinal vessels, depigmentation in non-tapetal area and optic disc atrophy with scalloped borders. Electroretinograms (ERG) recorded in 13 PRA-affected cases revealed non-recordable extinguished (flatline) ERG responses. A reduction mainly of a- and b-wave amplitudes in the ERG indicated a generalized photoreceptor disease.

摘要

在两年时间里,在印度繁育的犬类中发现了31例遗传性视网膜变性病例,主要怀疑为进行性视网膜萎缩(PRA),具有典型的初始夜盲病史,随后出现昼盲。在31只疑似患有PRA的犬中,8只(26%)年龄在1至5岁之间,15只(48%)在6至10岁之间,其余(26%)在11至15岁之间。最主要的品种是斯皮茨犬(18只,58%)。详细的眼科检查包括在适当情况下进行的泪液分泌试验、荧光素染色、压平眼压测量、裂隙灯生物显微镜检查和眼部超声检查。检眼镜和眼底镜检查的变化包括反光层区域的高反射性和变色、视网膜血管明显变细、非反光层区域色素脱失以及边界呈扇形的视盘萎缩。在13例受PRA影响的病例中记录的视网膜电图(ERG)显示为不可记录的熄灭(平线)ERG反应。ERG中主要是a波和b波振幅降低,表明存在广泛性光感受器疾病。

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本文引用的文献

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Mamm Genome. 2015 Dec;26(11-12):638-49. doi: 10.1007/s00335-015-9607-6. Epub 2015 Oct 29.
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Progressive retinal atrophy in the Polski Owczarek Nizinny dog: a clinical and genetic study.波兰低地牧羊犬的进行性视网膜萎缩:一项临床与遗传学研究。
Vet Ophthalmol. 2016 May;19(3):195-205. doi: 10.1111/vop.12284. Epub 2015 May 22.
3
A novel form of progressive retinal atrophy in Swedish vallhund dogs.瑞典瓦汉德犬中一种新型进行性视网膜萎缩。
PLoS One. 2014 Sep 8;9(9):e106610. doi: 10.1371/journal.pone.0106610. eCollection 2014.
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J Vet Med Sci. 2013 Oct;75(10):1303-8. doi: 10.1292/jvms.12-0358. Epub 2013 May 30.
5
Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration.全基因组关联研究在 RPGRIP1(-/-) 犬中确定了一个修饰基因座,该基因座决定了视网膜变性的发病时间。
Mamm Genome. 2012 Feb;23(1-2):212-23. doi: 10.1007/s00335-011-9384-9. Epub 2011 Dec 23.
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A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations.具有进行性视网膜萎缩的金毛寻回犬中的移码突变支持 SLC4A3 作为人类视网膜变性的候选基因。
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