Literature DB >> 20435980

New aspects of hereditary ataxia in smooth-haired fox terriers.

C Rohdin1, L Lüdtke, P Wohlsein, K Hultin Jäderlund.   

Abstract

Hereditary ataxia was diagnosed in three smooth-haired fox terrier puppies from Sweden, 25 years after the previous known case in the breed. In addition to the characteristic spinal cord pathology, brain involvement was evident clinically, in the form of behavioural changes and bilaterally decreased menace responses, and histopathologically, with degenerative changes in the brainstem. The striking similarities to hereditary ataxia in the Jack Russell terrier suggest the same disease process in both breeds. A common ancestor, a female dog born in 1951 and considered a carrier of the disease at that time, was found in both the maternal and paternal lines of the three puppies.

Entities:  

Mesh:

Year:  2010        PMID: 20435980     DOI: 10.1136/vr.b4821

Source DB:  PubMed          Journal:  Vet Rec        ISSN: 0042-4900            Impact factor:   2.695


  5 in total

1.  Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed.

Authors:  Oliver P Forman; Luisa De Risio; Cathryn S Mellersh
Journal:  PLoS One       Date:  2013-05-31       Impact factor: 3.240

2.  A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds.

Authors:  Cecilia Rohdin; Douglas Gilliam; Caroline A O'Leary; Dennis P O'Brien; Joan R Coates; Gary S Johnson; Karin Hultin Jäderlund
Journal:  Acta Vet Scand       Date:  2015-05-23       Impact factor: 1.695

3.  Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier.

Authors:  Alana Christina Gast; Julia Metzger; Andrea Tipold; Ottmar Distl
Journal:  BMC Vet Res       Date:  2016-10-10       Impact factor: 2.741

4.  A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1).

Authors:  Nico Mauri; Miriam Kleiter; Michael Leschnik; Sandra Högler; Elisabeth Dietschi; Michaela Wiedmer; Joëlle Dietrich; Diana Henke; Frank Steffen; Simone Schuller; Corinne Gurtner; Nadine Stokar-Regenscheit; Donal O'Toole; Thomas Bilzer; Christiane Herden; Anna Oevermann; Vidhya Jagannathan; Tosso Leeb
Journal:  G3 (Bethesda)       Date:  2017-02-09       Impact factor: 3.154

5.  Re-emergence of hereditary polyneuropathy in Scandinavian Alaskan malamute dogs-old enemy or new entity? A case series.

Authors:  Karin Hultin Jäderlund; Cecilia Rohdin; Mette Berendt; Øyvind Stigen; Merete Fredholm; Arild Espenes; Inge Bjerkås; Lars Moe
Journal:  Acta Vet Scand       Date:  2017-05-02       Impact factor: 1.695

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.