Chieffo C, Stalis I H, Van Winkle T J, Haskins M E, Patterson D F
Section of Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6010.
J Vet Intern Med. 1994 Mar-Apr;8(2):112-6. doi: 10.1111/j.1939-1676.1994.tb03207.x.
A syndrome of cerebellar Purkinje's cell degeneration and coat color dilution was diagnosed in a family of Rhodesian Ridgeback dogs. One male and 1 female from the same litter and 1 female from a different litter were evaluated for growth retardation, inability to ambulate, and progressive ataxia. On physical examination, lateral recumbency, severe ataxia, tremors, and diluted coat color were identified. Littermates with nondiluted coat color were neurologically normal. Results of routine laboratory tests, urine metabolic screenings, and karyotype analyses were normal. Histopathologic abnormalities at necropsy included cerebellar Purkinje's cell degeneration, reduced granular cell layer thickness, and uneven distribution of macromelanosomes within hair shafts. Pedigree analysis suggested an autosomal recessive mode of inheritance. This is the first description of a genetic syndrome affecting the central nervous system and associated with coat color dilution in dogs.
在一个罗德西亚脊背犬家族中诊断出一种小脑浦肯野细胞变性和被毛颜色变淡的综合征。对同一窝的1只雄性和1只雌性以及另一窝的1只雌性进行了生长发育迟缓、无法行走和进行性共济失调的评估。体格检查发现侧卧、严重共济失调、震颤和被毛颜色变淡。被毛颜色未变淡的同窝仔犬神经系统正常。常规实验室检查、尿液代谢筛查和核型分析结果均正常。尸检时的组织病理学异常包括小脑浦肯野细胞变性、颗粒细胞层厚度减少以及毛干内大黑色素体分布不均。系谱分析提示为常染色体隐性遗传模式。这是首次描述影响犬中枢神经系统并与被毛颜色变淡相关的遗传综合征。