POAG/PLL in the Shar Pei

POAG/PLL in the Shar Pei

We are delighted to report that the mutation causing primary open angle glaucoma (POAG) / primary lens luxation (PLL) in the Shar Pei has been identified at the Kennel Club Genetics Centre at the Animal Health Trust (AHT).
A test for this is now available through the Animal Health Trust DNA testing service

Shar Pei in profileShar Pei are known to suffer from primary open angle glaucoma (POAG) but have also been reported to be affected by primary lens luxation (PLL).
Primary glaucoma is a painful and blinding disease associated with high pressure inside the eye. It is an inherited condition and is subdivided into two types: primary open angle glaucoma (POAG) and primary closed angle glaucoma (PCAG).

In the Shar Pei both POAG and PLL appear to be caused by the same mutation.

In POAG/PLL, glaucoma results from reduced drainage of fluid from the eye. This causes a build-up of pressure which, in turn, leads to pain and blindness. The eyes become enlarged and the lens of the eye becomes wobbly or even falls completely out of its normal position. Most dogs become affected at approximately 4 – 6 years of age.

How common is the disease?

We do not yet know exactly how common POAG/PLL is in the Shar Pei but the condition is frequently encountered by veterinary ophthalmologists both in the UK and in the USA.

In the first 4 months of testing (1/3/2017-26/6/2017) we  tested 159 Shar Pei from 10 different countries.

21 dogs gave an affected result, 62 dogs gave a carrier result and 82 dogs gave a clear result

How is the disease inherited?

two Shar Pei pupsThe disorder shows an autosomal recessive mode of inheritance, which means that two copies of the defective gene (one inherited from each parent) have to be present for a dog to be affected by the disease.

Individuals with one copy of the defective gene and one copy of the normal gene, called carriers, show no signs of disease but can pass the defective gene onto their offspring.

When two carriers are crossed, 25% (on average) of the offspring will be affected by the disease, 25% will be clear and the remaining 50% will themselves be carriers.

Breeders using our  DNA test will be sent results identifying their dog as belonging to one of three categories.  In all cases the terms ‘normal’ and ‘mutation’ refer to the position in the DNA where this POAG/PLL mutation is located in the Shar Pei; it is not possible to learn anything about any other region of DNA from this  test.

CLEAR: These dogs have two copies of the normal gene and will not develop POAG/PLL as a result of the mutation we are testing for, although we cannot exclude the possibility they might develop a similar condition due to other causes or the effect of other, unidentified mutations.

CARRIER: these dogs have one copy of the mutation and one normal copy of DNA. These dogs will not develop POAG/PLL themselves as a result of the POAG/PLL mutation but they will pass the mutation on to approximately 50% of their offspring.

AFFECTED: these dogs have two copies of the POAG/PLL mutation and will almost certainly develop POAG/PLL during their lifetime.

We cannot exclude the possibility that carriers might develop a similar condition due to other mutations they might carry that are not detected by this test.

Quelle: https://www.ahtdnatesting.co.uk/tests/poagpll-dna-shar-pei/

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