Literature DB >> 8046673

Cerebellar Purkinje's cell degeneration and coat color dilution in a family of Rhodesian Ridgeback dogs.

C Chieffo1, I H Stalis, T J Van Winkle, M E Haskins, D F Patterson.   

Abstract

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.

Entities:  

Mesh:

Year:  1994        PMID: 8046673     DOI: 10.1111/j.1939-1676.1994.tb03207.x

Source DB:  PubMed          Journal:  J Vet Intern Med        ISSN: 0891-6640            Impact factor:   3.333


  7 in total

Review 1.  Cerebellar Abiotrophy Across Domestic Species.

Authors:  Erica Yuki Scott; Kevin Douglas Woolard; Carrie J Finno; James D Murray
Journal:  Cerebellum       Date:  2018-06       Impact factor: 3.847

2.  Late onset of cerebellar abiotrophy in a boxer dog.

Authors:  Sanjeev Gumber; Doo-Youn Cho; Timothy W Morgan
Journal:  Vet Med Int       Date:  2010-12-05

3.  Cerebellar granuloprival degeneration in an Australian kelpie and a Labrador retriever dog.

Authors:  Jonathan Huska; Luis Gaitero; Heindrich N Snyman; Robert A Foster; Marti Pumarola; Sergio Rodenas
Journal:  Can Vet J       Date:  2013-01       Impact factor: 1.008

4.  Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation.

Authors:  Oliver P Forman; Luisa De Risio; Jennifer Stewart; Cathryn S Mellersh; Elsa Beltran
Journal:  BMC Genet       Date:  2012-07-10       Impact factor: 2.797

5.  A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery.

Authors:  Kaisa Kyöstilä; Sigitas Cizinauskas; Eija H Seppälä; Esko Suhonen; Janis Jeserevics; Antti Sukura; Pernilla Syrjä; Hannes Lohi
Journal:  PLoS Genet       Date:  2012-06-14       Impact factor: 5.917

6.  MYO5A Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1.

Authors:  Matthias Christen; Madeleine de le Roi; Vidhya Jagannathan; Kathrin Becker; Tosso Leeb
Journal:  Genes (Basel)       Date:  2021-09-23       Impact factor: 4.096

7.  Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed.

Authors:  Joe Fenn; Mike Boursnell; Rebekkah J Hitti; Christopher A Jenkins; Rebecca L Terry; Simon L Priestnall; Patrick J Kenny; Cathryn S Mellersh; Oliver P Forman
Journal:  BMC Genet       Date:  2016-08-26       Impact factor: 2.797

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.