Archives for March 2021

The Veterinarian’s Corner: New Canine Genetic Disease Tests at Paw Print Genetics

The Veterinarian’s Corner: New Canine Genetic Disease Tests at Paw Print Genetics

As of January 2021, Paw Print Genetics (PPG) is proud to offer 44 new inherited disease tests for the canine health and breeding community. While these new tests are associated with diseases identified in dozens of breeds, the population size of each breed and the relative frequency of these mutations in those populations mean that some of these diseases are much more likely to be seen in clinical veterinary practice than others. Here we will highlight five diseases from the recent PPG test additions that are among those most likely to be diagnosed in the veterinary hospital setting.

Cerebellar Degeneration- Old English Sheepdog and Gordon Setter1

A genetic mutation in the canine RAB24 gene is associated with a juvenile-onset, autosomal recessive form of cerebellar degeneration (CD) in two seemingly disparate breeds, the Old English Sheepdog (OES) and Gordon Setter (GS). Also referred to as hereditary ataxia or cerebellar abiotrophy (CA), CD presents between 6 months and 4 years of age with progressive neurological dysfunction due to degeneration of cerebellar neurons, especially Purkinje neurons. Coordinated movement becomes progressively more difficult as the disease progresses and can include intention tremors, ataxia, and a stiff, high-stepping gait (hypermetria). Affected dogs are often ...

Testing for Dermatomyositis Risk

Testing for Dermatomyositis Risk

Dermatomyositis (DMS), also known as Juvenile Dermatomyositis or Canine Familial Dermatomyositis is an inflammatory disease of the skin and muscles caused by an over reactive immune system1. This disease has consistently plagued Shetland Sheepdogs and Collies of all varieties.  What makes this condition truly insidious is that although it mostly affects immature dogs, it can flare up seemingly out of nowhere to create issues in dogs of any age2.  Although testing for the genetic mutations that pre-dispose certain dogs for this disease has been around for some time, interpreting the results can be complicated often leaving owners confused about the results of this test.  Misunderstanding genetic results may lead to poor breeding decisions.  Let us look closer at DMS, how the disease presents, the complexity of genetic testing, and how to best utilize the results of this test.   

 

What is Dermatomyositis?

DMS is an inherited disease that causes dramatic inflammation of the skin, blood vessels and muscles in affected dogs.  Lesions often originate and are limited to the skin of the face with the lips with the area around the eyes particularly affected3.  Although the mechanisms of the ...

The Genetics of Hairlessness

The Genetics of Hairlessness
A hairless Chinese Crested next to a Powder puff

Aficionados of the hairless breeds are motivated to perpetuate and conserve these very historical and special dogs. The Xoloitzcuintles (“show-low-itz-QUEENT-ly.” or just Xolo “SHOW-low”) and the Chinese Crested dog are the more common hairless dogs but are no means the only hairless breeds. Some controversy surrounds the hairless breeds due to the nature of the hairless gene variant and its inheritance from one generation to the next. Looking at some basic genetics and how they apply to the inheritance of the mutation responsible for hairlessness will benefit the breeder trying to determine the best pairing for these unique dogs.


All genes are inherited from the parents. Half of the genetic material, or alleles, come from the mother, the other set of alleles come from the father. Two alleles, one from the dam and one from the sire, make up the genotype. The genotype will then determine the phenotype, or what trait or condition we observe in the dog. Further, we define genes as either being dominant or recessive. A dominant gene requires only one allele, passed from one parent, to express its phenotype. Whereas, a recessive gene requires two alleles, one passed from each parent, for its phenotype to ...