Blog Archives for the year 2014

Primary Hyperoxaluria: A Preventable Inherited Disease of the Coton de Tulear

Primary Hyperoxaluria: A Preventable Inherited Disease of the Coton de Tulear

There are not many dog breed names that give a more apt description of the breed’s physical appearance than that of the coton de Tulear. Taken from the French word “coton”, meaning cotton, the coton de Tulear’s signature soft white hair (not fur) has long been compared to the fluffy fiber of the cotton plant. According to the Malagasy Coton de Tulear Club of America, the coton de Tulear was developed in Madagascar around the 17th century and is still the official dog of this island nation. Predecessors to the modern coton de Tulear were likely brought to the island by sailors or pirates around this time period. Though they are generally a healthy breed, unfortunately, like other purebred dogs, the coton de Tulear is known to inherit some genetic diseases that can make life challenging for this small, friendly companion and those that love them. One such inherited disease of the coton de Tulear is a severe condition known as primary hyperoxaluria (PH) that occurs due to a mutation in the AGXT gene.

Dogs affected with PH lack the ability to produce an enzyme that plays an essential role in the breakdown of a compound known as glyoxylate ...

Testing for Progressive Retinal Atrophy, GR1 and GR2 Now Available for the Golden Retriever

Testing for Progressive Retinal Atrophy, GR1 and GR2 Now Available for the Golden Retriever

After many inquiries by our wonderful clients, Paw Print Genetics is excited to announce that we have begun testing for two genetic mutations reported to cause progressive retinal atrophy in the golden retriever. Known specifically as progressive retinal atrophy, GR1 and GR2 (PRA-GR1 and PRA-GR2), these two diseases were found to be caused by genetic mutations in the SLC4A3 and TTC8 genes, respectively. In addition to the golden retriever, the TTC8 mutation that causes PRA-GR2 has also been identified in a clinically affected Labrador retriever.

Progressive retinal atrophy (PRA) is not a single disease, but rather a group of inherited diseases each caused by different genetic mutations in different genes. The various forms of PRA affect over 100 different dog breeds. Though there are variations in the progression of disease, most varieties of PRA (regardless of genetic cause) result in blindness due to an inherited degeneration of the retina; more specifically, the degeneration of retinal cells known as rods and cones, which play an important role in vision.

In PRA-GR1 and PRA-GR2, signs of night blindness and loss of peripheral vision are seen first with progression to complete blindness occurring over time. In addition, they are both considered late onset ...

Hereditary Cataract Testing Has Arrived at Paw Print Genetics!

Hereditary Cataract Testing Has Arrived at Paw Print Genetics!

One of the hottest questions from our loyal, Paw Print Genetics clients over the past several months has been, “When are you going to offer genetic testing for hereditary cataracts?” After much preparation and anticipation, we are happy to report that Paw Print Genetics has begun testing for two different mutations of the HSF4 gene reported to cause hereditary cataracts (HC) in seven different breeds of dog.

Cataract is the term used to describe a condition in which opacities develop in the normally clear lens of the eye. The lens is responsible for focusing light onto the retina in the back of the eye resulting in acute, focused vision. With cataracts, the lens cannot focus light appropriately. This results in progressive vision deficits as the cataract increases in severity. While many cataracts identified in dogs are caused by non-inherited causes (e.g. UV radiation, infections, diabetes, chronic inflammation of the eye), as the name suggests, HCs are those passed from generation to generation. In addition, inherited genetic mutations are the most common cause of cataracts in dogs. However, by performing genetic testing on dams and sires prior to breeding, selective breeding precautions can be taken to prevent affected puppies ...

Progressive Retinal Atrophy (PRA1): A Preventable Inherited Disease of the Papillon and Phalène

Progressive Retinal Atrophy (PRA1): A Preventable Inherited Disease of the Papillon and Phalène

With their picturesque appeal, predecessors of the modern day papillon (known as continental toy or Titian spaniels) were popular subjects for European painters between the 16th and 18th centuries. The popularity of these small spaniels with European aristocrats and royalty of the Renaissance period, led to their appearance in many paintings from the era. The iconic, longhaired “butterfly-like” ears, for which papillons are named, are obvious in these paintings though many of the portrayed dogs were of the drop-eared variety of the breed that today is known as the phalène. According to an article on the Papillon Club of America website, in the late 19th century erect ears became a more desirable trait with papillon fanciers and eventually the erect-eared variety obtained their current position as the more popular form of the breed. In addition to their beautiful physical attributes, in their modern form, well-socialized papillons are described as happy, playful and affectionate family members. Papillons are also often described as frequent barkers, making them great guard dogs. Despite their adorable personalities and good temperament, like other purebred dogs, the papillon is known to inherit some genetic diseases that could prevent this regal breed from reaching the ...

Leukocyte Adhesion Deficiency: A Preventable Inherited Disease of the Irish Setter

Leukocyte Adhesion Deficiency: A Preventable Inherited Disease of the Irish Setter

From a thorough mixture of spaniels, pointers, and other setter breeds, the Irish setter made its rise to popular gun dog status in the 18th century in its native homeland, Ireland. Though originally of the red and white color pattern (now called the Irish red and white setter), by the time the Irish setter made its way to North America, the solid red color most commonly associated with the breed had been established through selective breeding practices. Originally bred for their versatility in hunting game birds, by the mid 1900’s the Irish setter’s role in the field had greatly diminished despite their popularity in the show ring. Controversial, yet successful, efforts were taken to outcross the breed to red and white champion English setters in order to preserve and improve field varieties. The resultant field variety, often referred to as the Red setter, is unique in its hunting abilities and appearance when compared to American show varieties of the Irish setter. However, the field variety still falls under the Irish setter name in the US.

Unfortunately, at some point during the breed’s development, a spontaneous mutation in the ITGB2 gene occurred in a single Irish setter. A portion of ...

Musladin-Lueke Syndrome: A Preventable Inherited Disease of the Beagle

Musladin-Lueke Syndrome: A Preventable Inherited Disease of the Beagle

While the history of the beagle’s early breed development has been lost due to lack of record keeping, the mid to late 1800’s saw the arrival of the modern beagle on the shores of North America. From its English homeland where it was developed to hunt rabbits and other small game, the beagle has become one of the most popular breeds in the United States, ranking 4th overall in the 2013 American Kennel Club’s registration statistics. Behind their charming, deep throated vocalization known as baying, lies a social, even tempered and jovial dog breed suited for modern family life. Unfortunately, like other purebred dogs, the beagle is known to inherit some genetic diseases that can dampen the spirits of this normally energetic and fun-loving breed. One such inherited disease of beagles is known as Musladin-Lueke syndrome (MLS), a multi-systemic disease of connective tissue.

Named after beagle breeders Tony and Judy Musladin and Ada Lueke, MLS was first reported in the 1970’s and has now been identified in multiple countries including England, Australia, America and Japan. In 2010, a genetic mutation in the ADAMTSL2 gene was found to be responsible for the unique clinical signs of this disease. Though not ...

The Newfoundland, the PICALM gene, and the SAS Controversy

The Newfoundland, the PICALM gene, and the SAS Controversy

Subvalvular aortic stenosis (SAS), one of the most common inherited cardiac diseases in dogs, is a major concern for many owners of large breed dogs including the Newfoundland, golden retriever, American Staffordshire terrier and Rottweiler. SAS is caused by an abnormal ring or ridge of tissue in the left ventricle of the heart resulting in a partial obstruction of the left ventricular outflow tract; the pathway that allows blood to flow from the left ventricle, through the aortic valve and into the aorta which carries oxygenated blood to the body. In mild cases, dogs live a normal life, free of clinical signs related to the vessel narrowing. However, in moderate to severe cases of SAS, the increased strain placed upon the heart to pump blood through the partially obstructed aortic valve can result in structural changes of the heart muscle, congestive heart failure, arrhythmias and sudden death. SAS also predisposes dogs to development of potentially lethal bacterial infections of the aortic valve. Unfortunately, it is not possible to predict the severity of disease in puppies by examining the hearts of affected parents. Mildly affected parents can have severely affected puppies and vice versa. On average, SAS-affected dogs only live to ...

Polyneuropathy: A Preventable Inherited Disease of the Greyhound

Polyneuropathy: A Preventable Inherited Disease of the Greyhound

From their ancient Egyptian roots depicted in carvings of their predecessors, the speed and agility of the greyhound has long fascinated humans who found great potential in the breed as hunting companions, and much later, as fantastic family dogs. Like other members of the large grouping of dog breeds known as sighthounds, it was obvious to their ancient human handlers that the greyhound’s exceptional athletic skill, lean muscular body, and keen vision could be invaluable for hunting both large and small game. While it is no longer as common for greyhounds to be used for hunting, their docile temperament outside of the hunt contributed to an easy transition to the more domestic lifestyle most greyhounds now live. Though able to run 40 miles per hour when properly conditioned, with regular exercise the greyhound is just as content taking it easy with their human family members. Despite their majestic appearance and impressive athletic attributes, like other purebred dogs, greyhounds are known to inherit some genetic diseases that may keep this talented runner at the starting block. One such disease, known as greyhound polyneuropathy (GP), is caused by a mutation in the NDRG1 gene.

GP is a severe, progressive neurological disease similar ...

Thrombopathia: A Preventable Inherited Disease of the Basset Hound

Thrombopathia: A Preventable Inherited Disease of the Basset Hound

Since the first exhibitions of the modern basset hound in the late 19th century, their mellow and charming personality has made them a popular family dog. Though according to the Basset Hound Club of America, it is not unusual for a basset hound to be a little stubborn or to have “selective hearing” (especially if following a scent trail), this minor annoyance is easily tempered by their affectionate and sensitive disposition. Originally bred for hunting with a person on foot, the basset hound’s short legs kept them from outrunning their handler while following their exceptional nose. Unfortunately, like other purebred dogs, the basset hound has also been unable to outrun susceptibility to certain inherited diseases. One such condition is a disease of blood platelets known as thrombopathia that occurs due to a mutation in the RASGRP1 gene.

Dogs affected with thrombopathia produce a dysfunctional form of a protein important in the aggregation of platelets during blood clotting. The resulting inability to produce functional blood clots leads to easy bruising and frequent episodes of spontaneous bleeding from the gums, nose, and the gastrointestinal tract. Affected dogs may also show signs of lameness due to spontaneous bleeding in joints. Loss of ...

Progressive Retinal Atrophy: An Inherited Disease of the English Springer Spaniel

Progressive Retinal Atrophy: An Inherited Disease of the English Springer Spaniel

The intelligent, prey-driven English springer spaniel (ESS) has forged its path as a popular, hardworking companion for bird hunters while maintaining a loyal and affectionate personality suitable to family life. Until the early 1900’s, springer spaniels were produced in the same litters as cocker spaniels; springers were chosen from the largest puppies of the litter and were trained for flushing or “springing” game while the smaller littermates were labeled cocker spaniels and were trained for hunting the elusive woodcock. Since then, springer spaniels have been further split into the generally leaner, shorter haired field (hunting) variety and the denser boned, densely haired show (“bench”) line. Unfortunately, like other purebred dogs, English springer spaniels are known to inherit genetic diseases that can keep some individuals from reaching the great potentials for which the breed is capable. One such inherited condition is an eye disease known as progressive retinal atrophy, cone-rod dystrophy 4 (PRA-crd4) caused by a mutation in the RPGRIP1 gene.

Progressive retinal atrophy (PRA) is not a single disease, but rather a group of inherited diseases each caused by different genetic mutations in different genes. The various forms of PRA affect over 100 different dog breeds. Though there are variations ...