Progressive retinal atrophy

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Progressive retinal atrophy (PRA) is a group of genetic diseases characterized by degeneration of the retina that occurs bilaterally. It is seen in certain breeds of dogs and more rarely, cats. It causes progressive vision loss culminating in blindness. The condition in nearly all breeds is inherited as an autosomal recessive trait, with the exception of the Siberian Husky (inherited as an X chromosome linked trait) and the Bullmastiff (inherited as an autosomal dominant trait).^[1] There is no treatment. PRA is similar to retinitis pigmentosa in humans.^[2]

Contents 1 Diagnosis 2 Types of PRA 2.1 Generalized PRA 2.2 Rod-cone dysplasia 2.2.1 Rod-cone dysplasia type 1 2.2.2 Rod-cone dysplasia type 2 2.2.3 Rod-cone dysplasia type 3 2.3 Rod dysplasia 2.4 Early retinal degeneration 2.5 Photoreceptor dysplasia 2.6 Cone degeneration 2.7 Progressive rod-cone degeneration (PRCD) 2.8 X-linked PRA 2.9 Dominant PRA 2.10 Feline PRA 2.11 Central progressive retinal atrophy (CPRA) 2.11.1 Commonly affected breeds 2.12 Hereditary retinal dysplasia 3 See also 4 References 5 External links

Diagnosis

Progressive vision loss in any dog in the absence of glaucoma or cataracts can be an indication of PRA. It usually starts with decreased vision at night, or nyctalopia. Other symptoms include dilated pupils and decreased pupillary light reflex. Fundoscopy to examine the retina will show shrinking of the blood vessels, decreased pigmentation of the nontapetal fundus, increased reflection from the tapetum due to thinning of the retina, and later in the disease a darkened, atrophied optic disc. Secondary cataract formation in the posterior portion of the lens can occur late in the disease. In these cases diagnosis of PRA may require electroretinography (ERG). For many breeds there are specific genetic tests of blood or buccal mucosa for PRA.^[1]

Types of PRA

Generalized PRA is the most common type and causes atrophy of all the neural retinal structures. Central progressive retinal atrophy (CPRA) is a different disease from PRA involving the retinal pigment epithelium (RPE), and is also known as retinal pigment epithelial dystrophy (RPED).

Generalized PRA can be divided into either dysplastic disease, where the cells develop abnormally, and degenerative, where the cells develop normally but then undergo a damaging change. PRA can be further divided into affecting either rod or cone cells. Rod cells detect shape and motion, and function in dim light. Cone cells detect color and definition, and function in bright light.

Generalized PRA

Commonly affected breeds:^[3]

• Akita - Symptoms at one to three years old and blindness at three to five years old.
• Miniature longhaired Dachshund - Symptoms at six months old.
• Papillon - Slowly progressive with blindness at seven to eight years old.
• Tibetan Spaniel - Symptoms at three to five years old.
• Tibetan Terrier - Symptoms at less than one year old, often blind by two years old, and cataract formation by four years old.
• Samoyed - Symptoms by three to five years old.

Rod-cone dysplasia

This type of PRA has an early onset of severe vision loss. It is caused by a defect in the gene for cGMP-phosphodiesterase, which leads to retinal levels of cyclic guanosine monophosphate ten times normal.^[4]

Rod-cone dysplasia type 1

• Irish Setter - Rod cell response is nearly absent. Night blindness by six to eight weeks old, often blind by one year old.^[3]
• Sloughi^[2]

Rod-cone dysplasia type 2

• Collie - Rod cell response is nearly absent. Night blindness by six weeks old, blind by one to two years old.^[3]

Rod-cone dysplasia type 3

• Cardigan Welsh Corgi^[2]

Rod dysplasia

• Norwegian Elkhound - Characterized by dysplasia of the rod cell unit and subsequent degeneration of the cone cell unit. Rod cell response is nearly absent. Night blindness by six months old, blind by three to five years old. This has been bred out of this dog.^[3]

Early retinal degeneration

• Norwegian Elkhound - Night blindness by six weeks old, blind by twelve to eighteen months old.^[3]

Photoreceptor dysplasia

This is caused by an abnormal development of both rod and cone cells. Dogs are initially night blind and then progress to day blindness.

• Miniature Schnauzer - Slowly progressive, not seen until two to five years old.
• Belgian Shepherd Dog - Complete blindness by eight weeks old.^[3]

Cone degeneration

• Alaskan Malamute - Temporary loss of vision in daylight (hemeralopia) at eight to ten weeks old. There is a purely rod cell retina by four years old.^[3]

Progressive rod-cone degeneration (PRCD)

This is a disease with normal rod and cone cell development but late onset degeneration of the rod cells that progresses to the cone cells. It is inherited as an autosomal recessive trait and has been linked to the ninth canine chromosome.^[2]

• Poodle - Night blindness by three to five years old, blind by five to seven years old.
• English Cocker Spaniel - Occurs late in life, usually at four to eight years old.
• American Cocker Spaniel - Night blindness by three to five years old, blind one to two years later.
• Labrador Retriever - Night blindness by four to six years old, blind at six to eight years old.
• Portuguese Water Dog^[3]
• Chesapeake Bay Retriever
• Australian Cattle Dog
• Nova Scotia Duck Tolling Retriever^[2]

X-linked PRA

This condition is linked to the X chromosome.

• Siberian Husky - Night blindness by two to four years old.^[3]
• Samoyed - More severe disease than the Husky.^[2]

Dominant PRA

• Bullmastiff - Inhertited as an autosomal dominant trait due to a mutation in the gene for rhodopsin.^[2]

Feline PRA

• Abyssinian - Two forms exist. One is inherited as an autosomal dominant trait and has an early age onset. The other is inherited as an autosomal recessive trait and has a middle age onset.^[2]
• Early onset PRA has also been reported in the domestic shorthaired cat and Persian. The Siamese also likely has a hereditary form of PRA.^[5] Despite belief among breeders to the contrary, there is apparently no link between coat color in Persians and the development of PRA.^[6]

Central progressive retinal atrophy (CPRA)

CPRA is also known as retinal pigment epithelial dystrophy (RPED). The cause of this condition is the loss of the retinal pigment epithelium's ability to effectively process the photoreceptor outer segment (POS) and subsequent accumulation of POS material in the RPE and loss of function. The loss of function of the RPE leads to photoreceptor degeneration.^[4] Vitamin E deficency may play a role in the development of CPRA.^[7] It is characterized by accumulation of pigment spots in the retina surrounded by retinal atrophy and a mottled appearance of the pigmented nontapetal fundus. The pigmented spots eventually coalesce and fade as the atrophy of the retina increases. It is an inherited condition (in the Labrador Retriever it is inherited as an autosomal dominant trait with variable penetrance).^[1] CPRA occurs in older dogs. Peripheral vision is retained for a long time. Vision is better in low light and better for moving or distant objects. Not all affected dogs go blind. Secondary cataracts are common.

Commonly affected breeds

• Labrador Retriever
• Golden Retriever
• Border Collie
• Collie
• Shetland Sheepdog
• English Cocker Spaniel
• English Springer Spaniel
• Chesapeake Bay Retriever
• Cavalier King Charles Spaniel
• Briard - has an especially high frequency.^[3]
• It can also, but very rarely, be found in the Papillon.^{[citation needed]}

Hereditary retinal dysplasia

There is another retinal disease in Briards known as hereditary retinal dysplasia. These dogs are night blind from birth, and day vision varies. Puppies affected often have nystagmus. It is also known as lipid retinopathy.^[3]

See also

• Sudden acquired retinal degeneration

References

Wikipedia information about Progressive retinal atrophy This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Progressive retinal atrophy". It may not have been reviewed by professional editors (see full disclaimer). Help contribute to Americola and edit this article.