We are lucky in our breed that there are
relatively few of the eye problems which plague collies and border collies
among other breeds. Normally if we clean the accumulated crud from the
corners of our beardies’ eyes each morning that pretty much covers eye care.
Occasionally we will notice a little pus amongst the crud and have to deal
with the infection. However, inherited eye problems do exist in beardies,
and lest we become complacent we need only look at the closely related
herding breeds and say there but for fortune… We are lucky in that we don’t
have to rely on Dame Fortune either. The eyes of all dogs used for breeding,
and preferably those of their closely related kin, should be checked by a
board certified ophthalmologist every two years at least. Only by careful
screening can we keep our breed’s eyes seeing clearly. It is sad that only
105 beardies underwent CERF examination in 2000. In this article I will look
at the inherited eye problems that have been reported in beardies as well as
some other non-inherited problems we may encounter. For only the second time
in the history of this column we have a diagram.

Inherited Diseases
Juvenile Cataracts
The lens of the eye is a soft, transparent structure that shortens or
lengthens to focus light beams on the retina at the back of the eye in order
for the eye’s owner to see objects sharply whether they are close or far
away. The capsule, a sort of sac, surrounds the lens, and supplies both
shape and nutrition to the lens, which is without blood vessels. Cataracts
are a cloudiness or opacity of the lens or capsule. Often people describe
cloudiness in the eyes of old dogs as cataracts, but this is rarely the
case. New fibers form at the periphery of the lens throughout life, to
compensate the fibers towards the centre become increasingly dense and
compact, this is called nuclear or lenticular sclerosis, this is not a
cataract and does not cause blindness. It does give the eye a grey or silver
cast. Cataracts can affect the whole eye or be localized. In beardies they are
usually found on the anterior surface of the lens (closest to the front of
the eye) at the top or bottom where the muscles attach to the capsule to
change the lens’ shape, and they are under the capsule. However, other
locations have been reported. While cataracts with genetic causes are
programmed at birth, most cases of juvenile cataracts in beardies are picked
up when the dog is between 2 and 5 years of age. The effect of these
cataracts on the beardie’s vision is usually mild, but bad enough that CERF
recommends that affected dogs not be bred. At this point too little is known
about the genetics of cataracts in beardies to speculate on the mode of
inheritance. In other breeds for which there is more data, cataracts may be
recessive, dominant or dominant with incomplete penetrance. In some breeds
cataracts can progressively increase in size until the animal is blind, this
has not been reported in beardies, although the degree of visual impairment
is variable. Cataracts can occur that are not of genetic origin, most common
causes are diabetes mellitus; infant/neonate milk replacement diets; uveitis
and altered aqueous humor composition; retinal degeneration; persistent
pupillary membranes; persistent hyaloid artery through the vitreous;
electric shock; radiation; and various toxins. Some cataracts cause the eye
to become inflamed and there will be excessive tearing and redness of the
sclera (white of the eye). The dog may seem to squint especially in bright
light. If left untreated this could progress to glaucoma or retinal
detachment.
If the eye becomes seriously inflamed or the dog is blind, surgery called
phacoemulsification sends ultrasonic shock waves through the eye to smash
the lens. Sometimes a plastic lens is placed in the eye, but this only
really improves near vision and is rarely helpful. Surgery results in 90-95%
restoration of functional vision.
Progressive Retinal Atrophy (PRA)
The retina at the back of the eye is composed of receptor cells called
rods and cones that respond by emitting nervous impulses when stimulated by
light of different wavelengths. Rods respond in dim light, whereas the
various types of cone respond to red, blue and green light. Not one but at
least 6 distinct inherited forms of PRA have been described in many breeds
of dogs and some mixed breeds. Ultimately PRA results in blindness. This is
not a common disease in beardies and I am not sure that the type of PRA seen
has been determined. In other breeds there is a test now for the gene
mutation in Irish setters that causes rod cone dysplasia 1 (rcd1), as well
as for a genetic marker for progressive rod cone degeneration (prcd). Prcd
is the most widespread form of PRA and is found in poodles, cockers
(American and English), labs, porties, Australian cattle dogs as well as
many other breeds. Dogs with prcd form normal retinas, but they start to
degenerate when the dog is about a year old, the dog first becomes night
blind and then totally blind usually between 3 and 5 years of age. Because
many dogs will have been bred before the disease can be detected the DNA
test is particularly important, and can be used to detect both carriers and
affecteds so that even the latter can be bred to clear mates so that puppies
will be carriers but not affected by prcd. Because the test is for a gene
marker rather than the mutation itself, the test may sometimes result in
false positives. PRA in Irish setters (rcd1) and in Norwegian Elkhounds (rod dysplasia
cone degeneration) is often apparent by the time the dogs are 6 weeks old,
have diminished vision by 12 weeks and are completely blind by the time they
are one or 2 years old.Because rods typically degenerate before cones the dog will be seen to
stumble and bump into things in dimly lit areas before doing so in bright
light. Their pupils tend to be dilated to catch as much light as possible.
Dogs with PRA have fewer blood vessels on their retinas. This initial
observation is followed up with an electroretinogram (ERG), which measures
the amplitude of electrical signals given off by the retinal cells. This
will be reduced in dogs with PRA.
In all breeds except the Siberian Husky, in which it seems to be a sex
linked recessive trait, PRA is an autosomal recessive problem, i.e. an
affected gene must be inherited from both parents. Without a genetic marker
it can remain hidden in the breed for a long time before suddenly cropping
up.
Retinal Dysplasia
This is a retinal malformation that occurs when two of the embryological
layers forming the retina fail to attach properly. In the mild form there
will be folding of the inner layer of the retina, appropriately called
"retinal folds". In the more severe form the layers do not attach at all,
and there is complete or partial retinal detachment. Retinal dysplasia is
not progressive, and can be detected in pups as young as 6 to 8 weeks old,
although with puppies that small and wiggly getting a good view of the
retina can be difficult. In most cases this is the result of a genetic
defect, however, prenatal infection with herpes or parvovirus may also be
causative. In many breeds simple autosomal recessive inheritance is
suspected, in others a single, autosomal dominant gene causes both retinal
dysplasia and skeletal changes. In many breeds, including beardies, there is
insufficient data to speculate on mode of inheritance.Retinal folds produce small blind spots that rarely affect overall vision
in dogs, but large areas or complete detachment result in major visual
defects to complete blindness. In breeds like beardies where the condition
is rare, and has not been found to produce major visual problems dogs with
retinal folds may still be given CERF certificates, but if large areas of
detachment exist the dog will not pass.
Retinal detachment is not necessarily hereditary. It can occur as a
result of trauma (penetrating wounds or foreign bodies to the eye as well as
blunt trauma), surgery to repair cataracts, or even spontaneously in dogs
with mature cataracts or lens luxation. Various infectious agents
(distemper, septicemia, bacteremia, leptospirosis, brucellosis, Rocky
Mountain spotted fever, ehrlichia, Lyme disease, parasitic larval migration,
toxoplasmosis, leishmaniasis, neospora and fungal and algal infections),
immune mediated vasculitis, idiopathic thrombocytopenia, systemic lupus
erythematosus and some toxic substances (griseofulvin - an antifungal agent,
timethoprim-sulfa – an antibiotic, ethylene glycol – antifreeze poisoning)
can all cause retinal detachment and subsequent blindness.
Persistent pupillary membranes (PPM)
These are a common finding in beardies, although at the last specialty
the ophthalmologist conducting the CERF exams decided that some of those
previously diagnosed in beardies were not PPM but actually "a normal
branched blood vessel in the inner and outer surface of the iris {the
colored part of the eye} which was closer to the surface than normal and
mimicked PPM". Currently PPM does not prevent a beardie from being given a
CERF certificate. PPMs are remnants of the fetal pupillary membrane that
covers the pupil before birth and provides a blood supply to the lens. In
puppies at birth the pupillary membrane is still present and is gradually
absorbed, normally disappearing by the time the puppy is four or five weeks
old. If you look at the pupils of pups whose eyes have just opened you may
see web like strands of the membrane.
When the strands don’t disappear they form PPMs. These may cross the
pupil from iris to iris, run from the iris to the lens, or iris to cornea,
or attach at one end to the iris with the other floating free. Strands can
be single or forked. Iris to iris PPMs rarely cause a problem, and may
continue to regress with age, but rarely disappear entirely. Those that
attach to the lens’ capsule though can result in small cataracts, opacities
on the lens, although these are non-progressive and rarely affect vision to
any significant extent. Worse are those attaching to the cornea where they
also produce opacity, but may also cause fluid to accumulate in the cornea (edema).
If there are a lot of strands this can lead to blindness. As pups age the
strands may regress and the blindness resolve, although the strands don’t
disappear completely. Iris to iris PPMs are classified by CERF as a "breeder
option" problem. Most are small and are probably sporadically occurring
rather than hereditary defects. Breeding these dogs does not produce puppies
with visual impairment. Breeding to unaffected dogs if possible may still be
advisable. This is the current status of PPMs in beardies. However, there
are breeds in which PPM is hereditary, and has been shown to produce
blindness in offspring. Any PPM seen in these breeds will result in denial
of a CERF certificate.
Distichiasis
Fortunately beardies aren’t affected by the more serious eyelid defects,
entropion and ectropion, where the eyelid rolls in or out, respectively.
Distichiasis describes the condition in which one or more eyelashes are
directed in towards the eye rather than outwards. If it is only one or two
eyelashes removing the offenders is sufficient. If there are more, surgery
is needed to correct the defect, which can produce conjunctivitis, and more
severe conjunctival abnormalities if left untreated. Usually in beardies
only a few hairs are involved. If the hair under the eyes is often stained
and you see an abundance of tearing, epiphora, you might suspect
distichiasis or possibly a blocked tear duct. The latter may require
surgical intervention.
Lipid corneal dystrophy
Is caused by the deposition of lipid in the body of the cornea. It is
seen in young adult beardies, although the pattern of inheritance has not
been determined. There is usually no inflammation or other symptom. Only in
cases of extensive depositions will vision be impaired. Usually there will
be a circular opacity in the center of the cornea that is grey, white or
silver in color. It is probably the result of a localized error in corneal
lipid metabolism, although elevated blood lipid levels can increase the size
of the opacities, which usually occur symmetrically in both eyes. Usually no
treatment is necessary. If the opacity interferes with vision then the lipid
can be surgically removed.
Hypertrophy of the nictitans gland of the third eyelid has been
reported as a hereditary problem in beardies. The third eyelid comes down
over the eye to help protect it, and you can normally spot it in the corner
of the eye. I have never come across this condition, but presumably it would
result in the third eyelid permanently prolapsing totally or partially over
the eye and would resemble the so-called "cherry eye", where the gland
detaches from the periorbit of the eye.
Non-inherited eye conditions
I’m only going to cover a couple of the more common problems. Tumors of
the eye itself (cancer of the orbit) are usually sarcomas or adenocanthomas
and most are primary and malignant. By the time they are normally detected
prognosis is poor. By contrast tumors of the eyelid are normally benign.
Red Eye
This is a general term used to describe a number of conditions that cause
swelling and redness of the eyelids, redness of the conjunctival membranes
(which line the eyelid and coat the white of the eyeball) or even hemorrhage
within the eye. It can also have a number of causes; these include
blepharitis (inflammation and swelling of the eyelids); conjunctivitis
(inflammation of the conjunctival membranes); keratitis (inflammation of the
cornea); inflammation of the sclera; anterior uveitis; glaucoma; disease of
the eyeball; or hyphema (blood in front of the iris). The first three
conditions are superficial and will involve superficial blood vessels in the
conjunctiva that have a lot of branching, deeper layers have less branching.
A discharge containing pus or pus and mucous also indicates a superficial
problem, while a clear, watery discharge indicates a deep problem. Blepharitis can be congenital in some breeds in which eyelid
abnormalities are inherited. In beardies causes would include trauma
(especially cat claw marks); allergy (atopy, food, insect bites, inhalant,
contact, drug, staph. hypersensitivity); autoimmune disease (pemphigus,
lupus); bacterial infection (causes a sty like appearance); fungal, viral or
parasitic infection; zinc or fatty acid deficiency; hypothyroidism,
hyperadrenocorticism or diabetes; neoplastic or a variety of other problems!
Clearly the first step is to find the cause rather than treat the symptom,
but a good first step would be to flush the eye with saline solution, apply
a warm washrag for 5-15 minutes 3 or 4 times a day, and clip the hair around
the eye. Further treatment depends upon the cause, but most bacterial
infections of the eyelid require systemic as well as topical antibiotics.Conjunctivitis is usually bacterial, but can also be viral, immune
mediated or neoplastic, the result of trauma or foreign body irritation or
secondary to dry eye or blockage of the tear ducts, a skin or other ocular
disease. If there is a serious discharge the eye should be cleansed as for
blepharitis and then the underlying cause addressed.Anterior uveitis is inflammation of the iris and/or the ciliary body,
which attaches the iris to the choroid, the brownish layer between the
sclera and retina. It is a common occurrence and has many causes including:
diabetes, hyperlipidemia (excessive fat in the blood); elevated blood
pressure; neoplasia (especially melanoma); cataracts; lens trauma or
rupture; immune mediated vasculitis; immune mediated thrombocytopenia;
algal, bacterial (including brucellosis, leptospirosis, Lyme disease or any
systemic infection), viral, fungal or protozoal infection; trauma –
especially blunt penetrating injuries; radiation; or blood clotting
disorder. All cases of anterior uveitis should be rigorously investigated to
discover the underlying cause. Topical +/-subconjunctival steroid or
non-steroidal anti-inflammatory drugs are indicated in severe cases. Other
treatment is cause dependent.Glaucoma is an increase in pressure within the eye as a result of reduced
drainage of aqueous humor; this may be inherited and result from a narrowed
drainage channel or secondary to another eye problem - lens luxation,
anterior uveitis or hyphema. Inherited glaucoma has not been reported in
beardies. It is a painful condition, the cornea is cloudy, the pupil dilated
and there is a sudden loss of vision. As the disease progresses the eye will
start to bulge. While treating the underlying cause is important, topically
applied timolol reduces the production of aqueous humor; a diuretic may also
be administered. Mannitol may be used to dehydrate the vitreous humor. In
dogs in which anterior uveitis is not the inciting factor pilocarpine is
applied to constrict the pupil and improve flow of aqueous humor.
Hyphema - blood in the aqueous humor - can result from trauma, retinal
detachment, a tumor of the iris, ciliary body or choroid; uveitis especially
from a rickettsial infection (ehrlichia, RMSF); blood clotting disorder;
immune mediated vasculitis; systemic high blood pressure – either primary or
secondary to kidney disease; or abnormal parasite migration. Treatment of
the causative factor is indicated.
Corneal ulcers, degeneration and infiltration
These all cause opacity of the cornea. Ulcers are the result of erosion
of the cornea secondary to inflammation. Ulcers can be superficial or deep
and may be complicated by infection or the presence of degradative enzymes
that can cause "melting" of the cornea and rapid spreading of the ulcer. In
beardies trauma or foreign bodies in the eye are probably the most likely
cause of ulcers, although dry eye, distichiasis, infection or paralysis of
the eyelid - so that the cornea is not coated with tears and becomes dry and
brittle - are all possible. Ulcers are diagnosed by applying fluorescein
dye, which they retain. Topical antibiotics are usually applied as well as
acetylcysteine to prevent "melting" ulcers. Therapeutic contact lenses may
act as a kind of bandage to protect the healing cornea. Topical
corticosteroids should not be applied. To repair deep ulcers surgical
placement of a flap of conjunctival tissue may give the best chance of
success. The cornea may be inflamed and yet not retain fluorescein. The
cornea may become stained pinkish white and the eye is often painful causing
tearing, squinting, blinking and rubbing at the eye. Nonulcerative
inflammation of the cornea is probably immune mediated and treatment is
directed at managing the signs rather than at producing a cure.Corneal degeneration or infiltration by lipid or calcium deposits is not
inherited, and distinct from corneal lipid dystrophy. Lipid deposits are
seen most often in dogs that are hypothyroid. There’s usually an associated
inflammation, blood vessels and pigmentation also appear. The deposits are
grey or white and may be circular, arced or irregular. The condition may
progress to form ulcers and these should be treated accordingly, as should
any underlying causative condition. A low fat diet may reduce lipid
deposition. If the dog appears painful or its vision is impaired scraping
the cornea or removing the outer layer of the cornea will help resolve the
condition.
The eyes are the windows of the soul. I have barely scraped the surface
in looking at potential problems, and yet as I said at the beginning our
beardies are fortunately not plagued with major ophthalmic problems, and we
should do everything we can to keep it that way. Which leads to the question
that I’m sure everyone who’s stuck with me thus far is dying to ask. Should
we tie back our beardies’ hair or let it flop over their eyes. Obviously the
answer is … it depends. The original beardies had far less hair than our
heavily coated dogs do now, their hair flopped down and protected their eyes
from trauma as they ran through gorse and bushes, it kept out dust and mud
and too bright sun. Now if our dogs are bumping into things all the time, or
really need to see well, to avoid bumping the top rail of a jump, tying
their hair back is an advantage. If my beardies are anything to go by, you
can tie back most of the hair, but within a short while wisps will break
away and flop down over the eyes providing enough cover to help shield the
eyes from sticks and dust, but not enough to seriously impede their vision,
and that is probably about the way it should be. I don’t like trimming the
hair away as I think it does make the eyes more vulnerable, thinning is an
option some people take, and if it’s not a show dog there’s no harm in that,
in my opinion.
Copyright © 2002 [ Linda Aronson DVM].
All rights
reserved
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