Literature DB >> 25441626

Canine hereditary ataxia.

Ganokon Urkasemsin1, Natasha J Olby2.   

Abstract

The hereditary ataxias are a group of neurodegenerative diseases that cause a progressive (or episodic) cerebellar ataxia. A large number of different disorders have been described in different breeds of purebred dog, and in some instances, more than one disorder occurs in a single breed, creating a confusing clinical picture. The mutations associated with these disorders are being described at a rapid rate, potentially changing our ability to prevent, diagnose, and treat affected dogs. A breed-related neurodegenerative process should be suspected in any pure bred dog with slowly progressive, symmetric signs of ataxia.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cerebellar abiotrophy; Granuloprival degeneration; Purkinje neuron; Spinocerebellar

Mesh:

Year:  2014        PMID: 25441626     DOI: 10.1016/j.cvsm.2014.07.005

Source DB:  PubMed          Journal:  Vet Clin North Am Small Anim Pract        ISSN: 0195-5616            Impact factor:   2.093


  10 in total

1.  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

2.  Genetics of Hereditary Ataxia in Scottish Terriers.

Authors:  G Urkasemsin; D M Nielsen; A Singleton; S Arepalli; D Hernandez; C Agler; N J Olby
Journal:  J Vet Intern Med       Date:  2017-05-29       Impact factor: 3.333

3.  A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2).

Authors:  Nico Mauri; Miriam Kleiter; Elisabeth Dietschi; Michael Leschnik; Sandra Högler; 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:  2017-08-07       Impact factor: 3.154

4.  A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia.

Authors:  Anna Letko; Elisabeth Dietschi; Marco Nieburg; Vidhya Jagannathan; Corinne Gurtner; Anna Oevermann; Cord Drögemüller
Journal:  Genes (Basel)       Date:  2019-05-10       Impact factor: 4.096

5.  Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs.

Authors:  Christopher A Jenkins; Lajos Kalmar; Kaspar Matiasek; Lorenzo Mari; Kaisa Kyöstilä; Hannes Lohi; Ellen C Schofield; Cathryn S Mellersh; Luisa De Risio; Sally L Ricketts
Journal:  PLoS Genet       Date:  2020-01-30       Impact factor: 5.917

6.  A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia.

Authors:  Marie Abitbol; Vidhya Jagannathan; Nelly Laurent; Eglantine Noblet; Guillaume F Dutil; Thibaut Troupel; Caroline de Dufaure de Citres; Vincent Gache; Stéphane Blot; Catherine Escriou; Tosso Leeb
Journal:  Anim Genet       Date:  2022-07-21       Impact factor: 2.884

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

8.  Transient Postural Vestibulo-Cerebellar Syndrome in Three Dogs With Presumed Cerebellar Hypoplasia.

Authors:  Miroslav Prikryl; Abby Caine; Viktor Palus
Journal:  Front Vet Sci       Date:  2020-08-05

9.  A 1 bp deletion in HACE1 causes ataxia in Norwegian elkhound, black.

Authors:  Kim K L Bellamy; Fredrik S Skedsmo; Josefin Hultman; Ellen F Arnet; Ole Albert Guttersrud; Hege Kippenes Skogmo; Stein Istre Thoresen; Arild Espenes; Karin Hultin Jäderlund; Frode Lingaas
Journal:  PLoS One       Date:  2022-01-21       Impact factor: 3.240

10.  Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs.

Authors:  Matthias Christen; Sandra Högler; Miriam Kleiter; Michael Leschnik; Corinna Weber; Denise Thaller; Vidhya Jagannathan; Tosso Leeb
Journal:  PLoS Genet       Date:  2021-08-02       Impact factor: 5.917

  10 in total

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