Cookies on VetMed Resource

Like most websites we use cookies. This is to ensure that we give you the best experience possible.

 

Continuing to use www.cabi.org  means you agree to our use of cookies. If you would like to, you can learn more about the cookies we use.

VetMed Resource

Veterinary information to support practice, based on evidence and continuing education

Sign up to receive our Veterinary & Animal Sciences e-newsletter, book alerts and offers direct to your inbox.

Results per page:

Search results

Abstract

Animals that have inherited a mutant gene from their parents (father and/or mother) may acquire hereditary diseases. Most mutations are autosomal recessive. Usually, hereditary diseases go unnoticed until symptoms arise. The objective of this study is to screen four canine hereditary diseases in...

Author(s)
Kuo RueiJia; Liu ChenHsuan; Hsieh ChinFong; Jiang JiaWei; Liao TaiChing [Liao, T. C. A. ]
Publisher
Chinese Society of Veterinary Science, Taipei, Taiwan
Citation
Taiwan Veterinary Journal, 2017, 43, 4, pp 277-284
AbstractFull Text

Genomic research of hereditary diseases is highly significant in the development of specific diagnostic markers meant to identify dogs carrying gene mutations. The Online Mendelian Inheritance in Animals database shows that there are 324 Mendelian disorders in dogs, of which 247 have their likely...

Author(s)
Cocostîrc, V.; Pusta, D. L.
Publisher
University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Romania
Citation
Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Veterinary Medicine, 2020, 77, 1, pp 9-14
CABI Book Chapter Info
Cover for Medical genetics.

This chapter describes the genetic risk factors and mode of inheritance of hereditary diseases in horses.

Author(s)
Bailey, E.; Brooks, S. A.
ISBN
2020 CABI (H ISBN 9781786392589)
Type
Book chapter
Abstract

There are several known hereditary diseases in Arabian horses. Many studies have been conducted on molecular diagnostic methods of the mutations that cause these hereditary defects in horses. A five-base deletion in the short arm (ECA9p12) of the equine chromosome 9, starting with codon 9480, which ...

Author(s)
Doğan, M.; Kaya, M.
Publisher
TÜBITAK, Ankara, Turkey
Citation
Turkish Journal of Veterinary & Animal Sciences, 2020, 44, 3, pp 729-733
Abstract

Congenital, familiar or inherited diseases of upper and lower urinary tract includes a big variety of diseases that may make changes in any part of the urinary tract itself. Some of these diseases are well genetically defined, and specific tests are available to diagnose the affected and the...

Author(s)
Brovida, C.
Publisher
Point Veterinaire Italie s.r.l., Milan, Italy
Citation
Summa, Animali da Compagnia, 2020, 37, 2, pp 5-14
Abstract

Megacolon is a hereditary disease of rabbits with spotted phenotype related to hypomotility and dilatation of cecum and colon with formation of abnormally large feces. This article describes the clinical case of cecum hypomotility in the rabbit, which has been presented with signs of abdominal...

Author(s)
Jekl, V.; Hauptman, K.
Publisher
Profi Press, s.r.o., Praha 2, Czech Republic
Citation
Veterinářství, 2019, 69, 5, pp 284-290
AbstractFull Text

The objective of this study consisted in a screening of the main hereditary diseases BLAD, DUMPs and Citrullinaemia using the GGP-BovineLDv3 panel in a representative population of Holstein heifers of the eastern area of Uruguay, as well as the analysis of BLAD mutant allele frequency since it was...

Author(s)
Sica, A. B.; Federici, M.; Dutra, F.; Briano, C.; Romero, A.; Rizza, M. dalla; Llambí, S.
Publisher
Sociedad de Medicina Veterinaria del Uruguay, Montevideo, Uruguay
Citation
Veterinaria (Montevideo), 2018, 54, 210, pp 9-13
Abstract

This article describes the value of genetic testing to screen for hereditary diseases in different dog breeds.

Author(s)
Malm, S.
Publisher
Sveriges Veterinärförbund, Stockholm, Sweden
Citation
Svensk Veterinärtidning, 2019, 71, 5, pp 12-15
Abstract

This article describes the genetic origins and genetic testing for progressive retinal atrophy (PRA) and several hereditary diseases that occur in many different dog breeds that result in blindness.

Author(s)
Janson, M.
Publisher
Sveriges Veterinärförbund, Stockholm, Sweden
Citation
Svensk Veterinärtidning, 2019, 71, 5, pp 28-32
Abstract

Both dogs and humans suffer from hereditary diseases such as impaired vision and blindness. Children and young people can also have Stargard's disease, one of the most common forms of hereditary retinal degeneration. An international team composed of researchers from SLU has initiated a mutation in ...

Author(s)
Janson, M.
Publisher
Sveriges Veterinärförbund, Stockholm, Sweden
Citation
Svensk Veterinärtidning, 2019, 71, 5, pp 34

Refine Results

Sort Order
Author
Geographical Location
Item Type
Language
Organisms
Subject Topics

Datasheet Filter