Disorders in Arabian Horses
WORLD ARABIAN HORSE ORGANIZATION
GENETIC DISORDERS IN ARABIAN HORSES: CURRENT RESEARCH PROJECTS
the important news updates on Cerebellar Abiotrophy and Lavender Foal Syndrome has been added to the end of this article,
INTRODUCTION: Researchers have already identified over 13,000 genetically
inherited traits in humans, more than 5,000 of them are diseases or other abnormalities. Many of these diseases also occur
in animals including horses of all breeds, world-wide, so Arabians are not the only breed of horse to have problems with inherited
disorders, which may be fatal or disabling genetic conditions. However, some genetic disorders are breed specific and in this
short article we will be looking only at the most serious genetic disorders which are known to affect Arabian horses.
is important to understand that inherited genetic disorders in Arabian horses know no boundaries. They have been reported
in all blood lines of the Arabian breed and reported cases have come from almost all countries where Arabians are being bred
today. It is also important to understand that there is nothing to be gained from “pedigree witch-hunts”. Through
science, we can all learn to deal with facts as they are today, and not to ‘point fingers’ at individual horses
from the past which may or may not have been the original sources of these genetic disorders. It also has to be said that
it may not be possible or wise to eliminate a genetic disorder altogether, because by doing so an unwanted side effect might
be to also eliminate other beneficial traits and diminish, rather than enhance, the gene pool.
It is to all our benefit
to become more informed about the genetic disorders in our Arabian horses, to support the researchers in their work and whenever
possible to take the necessary steps to selectively avoid the production of affected foals. By identifying the genes responsible
and having gene tests available, these can be used as tools by responsible owners when planning breedings, so that carriers
are not bred to carriers. In this way affected foals, with all the attendant heart-break that this causes to their breeders,
would not be produced.
Fortunately, a few Universities around the world are still undertaking research in an attempt
to create gene tests to identify carriers of the many inherited equine genetic disorders, not only those found in Arabians.
The Equine Genome Project is now complete, and a full ‘map’ of the horse’s genes is now available to researchers.
Universities also hold vast databanks of DNA, much of it from registered and parent-verified horses of many breeds, with known
pedigrees going back generations. These databanks hold the key to the future of equine gene test research.
It is only
through the collection of large numbers of samples that these genetic diseases can be studied; the location of the mutant
allele established and a genetic carrier test developed, as has been done for SCID. Then, and only then, will breeders have
the ability never to breed an affected foal again. This is the ultimate goal of the researchers which will benefit us all.
The research teams need to obtain samples from affected foals in order to carry out their work. Owners and breeders of affected
horses are being asked to submit samples both from the affected animal(s) and if possible from their related family members,
together with their registered identification. It is important to note that these Research Centres all have confidentiality
clauses in their sample donation forms so the identity of the affected animals, their pedigrees, breeders and owners are protected
against any type of finger pointing or 'witch-hunt' against any particular blood-line, which was an unfortunate side-effect
of the early research into SCID.
The main reason that this research is taking so long is financial, it is extremely
time consuming and expensive to identify the specific genes which cause these disorders, especially when it is into the relatively
rare conditions such as Lavender Foal Syndrome, and it will not be successful without further funding. Anyone who wishes to
make a donation towards this research should contact the WAHO Office for further information. Please support this research.
All communications are welcomed. All information is confidential.
GENETIC DISORDERS IN THE ARABIAN BREED: There are
four known genetic conditions in Arabian horses, which usually result in death or euthanasia of the affected animal. All four
are thought to be autosomal recessive conditions, which means that the flawed gene is not sex-linked and has to come from
both parents for an affected foal to be born. A fifth genetic condition, Juvenile Epilepsy Syndrome is not usually fatal,
but can be disabling if not treated.
- Severe Combined Immunodeficiency Disorder
- Cerebellar Abiotrophy (CA);
- Lavender Foal Syndrome (LFS);
- Occipital Atlanto-Axial Malformation
- Juvenile Epilepsy Syndrome (JES).
1. Severe Combined Immunodeficiency Disorder (SCID). After many decades
of expensive and time-consuming research, the good news is that for some years there has been a DNA test available, developed
by VetGen in America, that can detect whether a horse is clear of the SCID gene, is a carrier of SCID gene, or is an affected
foal which has inherited the gene from both parents. A horse which carries one copy of the SCID gene is not affected and is,
to all intents and purposes, healthy.
SCID is known to be an autosomal recessive trait and is found in many mammal
species. "Autosomal" means the trait is not sex linked, and "recessive" means that in order for a foal to be affected, it
must have 2 copies of the mutated allele, receiving one copy from each parent. A foal affected by SCID is born with no immune
system, and generally dies of an opportunistic infection such as pneumonia, usually before the age of five months. Breeders
who suspect SCID can have the foal or both parents gene tested, and if positive may opt for early euthanasia of an affected
foal to prevent further suffering.
Since SCID is an autosomal recessive disease, matings between two clear animals
as well as matings between a clear and a carrier animal will never produce an affected animal. By definition, carriers of
genes for autosomal recessive disorders are completely free of clinical signs of the disease. That is, carriers do not have
any negative consequences to their health or performance. Responsible owners are declaring the SCID status of their stallions
and generally require that mares sent to those stallions are tested as SCID clear prior to breeding. Please note there is
no reason that SCID carriers should not be used for breeding provided care is taken not to breed carrier to carrier. WAHO
does not at this time support any proposition that SCID carriers should be formally excluded from breeding by any Member Registry.
Through responsible SCID testing and avoiding breeding carrier to carrier, owners can now eliminate the possibility of an
affected foal ever being born.
The majority of WAHO Member Registries can now advise their members and owners of their
nearest recognized laboratory offering SCID testing, of which there are now several world-wide, so a full list will not be
reproduced here. Alternatively, please contact the WAHO Office for further information.
USEFUL CONTACTS FOR SCID INFORMATION:
Plaza Drive, Suite 1
Tel: +1-734-669-8440 Fax: +1.734.669.8441
Website: http://vetgen.com (There are many excellent articles on SCID available at this website)
Marguerite Illing, Treasurer
853 Cooley Road
Parksville, NY 12768-5336
2. Cerebellar Abiotrophy (CA) also referred to as cerebellar cortical
abiotrophy (CCA), is a neurological disease affecting the neurons known as Purkinje cells in the cerebellum of the brain,
causing them to die off. With CA, the Purkinje cells do not regenerate and once atrophied, their useful life is lost permanently.
These cells affect balance and coordination. Put simply, without Purkinje cells, an animal loses its sense of space and distance,
making balance and coordination difficult. In most cases, the neurons begin to die off shortly after the animal is born and
the condition is noticeable when the animal is less than six months old, though sometimes the onset of symptoms is gradual
and the animal is much older before the owner or caretaker notices a problem. Cerebellar Abiotrophy is different from Cerebellar
Hyperplasia. Research since 1967 indicates that CA is thought to be an autosomal recessive mode of inheritance.
affected foal is usually born without any clinical signs, but after 6 weeks and even as late as 18 months the following notable
symptoms may be observed: A palsy-like head shaking called ‘intention tremors’ affecting only the head and not
the neck or body, particularly noticeable when the foal is trying to focus on something; the lack of a normal blink response
although vision is correct; and an awkward exaggerated form of action with the forelimbs called ‘hyper-metric action’
similar to a military goose-step or high elevation used to cross over a very low object. Sometimes in a badly affected individual
it appears that the hind legs are also affected, but not usually. This hyper-metric action involves a shooting out and up
of the foreleg directly from the elbow at both the walk and the trot. The hoof is brought down to the ground with a thump,
often heel first. When cantering on level ground the horse looks as if it is cantering uphill, like a butterfly stroke in
swimming. It is a highly exaggerated gait. The more stressed the horse, the more exaggerated the gait. Their spinal column
is not involved; they do not lose weight; they are not in pain; they are neither lethargic nor show signs of increasing weakness,
or loss of muscle tone.
As these affected foals will often run into things or fall down, sometimes causing head injuries,
their condition can be misdiagnosed as injuries from a blow to the head or neck, making the true neurological condition go
unnoticed. A CA affected horse has little to no control over its balance and has difficulty judging distances between itself
and an object. Hence, they startle easily and appear panicky and hyper-active. When maintained in a constant environment,
the older the horse or foal becomes the more it adapts to the surroundings and its own disabilities, thus appearing as if
it is improving. Change the environment and the affected horse will have to undergo a serious of hopefully minor 'accidents'
before it has adapted to the new distances and objects. Often an older affected horse will have a 'horse buddy’, which
will be their guide. Horses with CA will often be referred to mistakenly as 'Wobblers', which is a condition of the spinal
cord, not of the brain, or are misdiagnosed as a head injury caused by an accident. The degree of severity varies, with some
foals having fast onset of severe coordination problems, others showing milder symptoms. In theory, mildly affected horses
could live a full lifespan, but in practice, most are euthanized before adulthood because they are so accident-prone as to
be a danger to themselves and others. They are not safe to ride.
Although the clinical signs are distinctive, the
only way to confirm a diagnosis of CA is to examine the brain after euthanasia. There is currently no genetic test for CA
but extensive research to identify the gene and create such a test is now under way in USA and Europe. To enhance and speed
research, UC Davis and the Swiss Genetics Institute have agreed to exchange data information on gathered samples, thus expanding
knowledge for both research centers. This also facilitates the mailing of samples to the nearest research centre.
FOR CURRENT RESEARCH INTO CA:
Penedo PhD., Geneticist.
Veterinary Genetics Laboratory
University of California
One Shields Avenue
Dr. Penedo is carrying on the research started by the late Dr. Ann Bowling, well-known author and geneticist, whose
studies in 1984 were unable to be published prior to her untimely death. Dr. Penedo has very recently identified the chromosome
(locus) which holds the mutant allele and is now researching the genes within that area.
Foal Syndrome (LFS), also called Coat Color Dilution Lethal (CCDL). Lavender foals are characterized by an unique coat colour
and neurological dysfunction which leaves them unable to stand. The mode of inheritance has not been established although
some researchers feel that it is an autosomal recessive. Because LFS is relatively rare, there is little in the veterinary
literature about it and there is currently no genetic test for LFS. Some research appears to indicate this syndrome may be
due to a biochemical lesion of the central nervous system involving the release of lower motor neurons but this is not yet
The most striking feature of LFS affected foals is that they are born with a coat color dilution that lightens
the tips of the coat hairs, or even the entire hair shaft. Coat color is a dull pinkish-gray, the hairs may be somewhat silvery
and the skin tends to be an unhealthy pink color. In a few cases, the coat colour is a very unusual iridescent silver to pale
lavender blue. Some affected foals do not exhibit this particular colour, but are unusually pale compared to normal foals.
Hence the description ‘lavender’ refers to this unique colour at birth, but Coat Colour Dilution is probably a
more accurate description.
In many cases, foals have had a difficult delivery (dystocia) and all LFS foals are never
able to stand and nurse. Foals may therefore be misdiagnosed as having neonatal maladjustment syndrome, also known as "dummy"
foals, due to a lack of oxygen from the dystocia, or the symptoms may appear similar to spinal cord injury, but the LFS affected
foal is generally distinguished from these by the peculiar coat colour.
The neurological dysfunction is characterized
by opisthotonus, a position where the head and neck are drawn back, with the body and legs rigid, and is accompanied by convulsions
or spasms. This condition is due to a disturbance of the central nervous system. Although unable to right itself, an LFS foal
may have a strong suckle reflex and may be bottle fed, however this is usually to no avail. Nystagmus or involuntary, rapid
eye movements are a secondary sign of opisthotonus and is present in some LFS foals. Foals with LFS often have seizures, and
if they do not die they are usually euthanized within a few days of birth on humane grounds as they are incapable of survival.
LFS should be considered a possibility in the differential diagnosis of any newborn Arabian foal with a markedly dilute
coat colour exhibiting a seizure-like disorder at birth.
Research to find the LFS gene is already underway at Universities
in USA and Australia, but urgently needs further funding. By comparing the clinical signs of Lavender foals with similar syndromes
in other species, several genes have been identified as good candidates for harboring a mutation that might cause Lavender
Foal Syndrome. The researchers would welcome submission of any samples.
CONTACTS FOR RESEARCH INTO LFS:
Horse Society of Australia is actively promoting the LFS research project getting underway at the University of Queensland.
There are also ongoing smaller research projects in USA. Anyone interested in helping with these projects, either through
funding donations, or by submitting samples from affected foals, should contact:
Locked Bag No. 6. 226 George Street
Windsor, N.S.W. 2756
Tel: +61 (0) 2-45-775-366 Fax:
+61 (0) 2.45.877.509
and ask to be put in touch with:
Dr Glen Coleman at the University of Queensland, Australia (email: email@example.com)
Or: Professor Dr. Tom E. Broad, Director, Australian Equine Genetics Research Centre, Brisbane
The Equine Genetics Center, James A. Baker Institute for Animal Health
College of Veterinary Medicine, Cornell
Ithaca, NY 14853, USA
Tel: +1-607-256-5621, Fax: +1-607-256-5608
F.O.A.L. website (see above under SCID contacts) also has an interesting article on Lavender Foal Syndrome and some research
being done by Dr. Penedo at UC Davis in California (for address see above under CA contacts).
There is also
a smaller research group directed by Professor Jim Moore DVM, PhD, Dip ACVS,
Department of Large Animal Medicine,
College of Veterinary Medicine,
University of Georgia,
Athens, GA 30602-7385,
Occipital Atlanto-Axial Malformation (OAAM). This is a condition where the cervical vertebrae fuse together in the neck and
at the base of the skull. Symptoms range from mild in-coordination to the paralysis of both front and rear legs. Some affected
foals cannot stand to nurse, in others the symptoms may not be seen for several weeks. This is the only cervical spinal cord
disease seen in horses less than 1 month of age, and a radio-graph can diagnose the condition. There is no genetic test for
OAAM, and the hereditary component of this condition is not well researched at present. There are some researchers who feel
that it is also an autosomal recessive.
Any breeder with an affected foal should contact their own Registering Authority
or Breed Society or nearest Veterinary College in the first instance, to find out if there are any research projects known
of in their region. At this time WAHO Office has been unable to locate any specific research projects.
Epilepsy Syndrome (JES), sometimes referred to as "benign" epilepsy or "idiopathic" epilepsy, is not usually fatal. Foals
are born normal and appear normal between epileptic seizures, usually outgrowing the condition between 12 and 18 months. Affected
foals may show signs of epilepsy anywhere from two days to six months from birth. Most foals will have what is called 'cluster
seizures'. Usually occurring before the third month birthday these are multiple seizures over a three day period with signs
of confusion, blindness, head rubbing, depression, inability to eat, nurse or even drink. Affected foals may suffer serious
injury as a result of falling to the ground, against hard objects or into fences. The more severe Grand Mal seizures may cause
the horse to lose consciousness and the eyes roll back into the head.
Researcher Dr. Monica Aleman at UC Davis in
California has pointed out that a foal cannot be considered to have epilepsy unless it has had more than two seizures. Close
observation is essential as some seizures may be slight. The mode of inheritance for Juvenile Epilepsy Syndrome has not yet
been determined. However, there are different theories at present; one suggests that, like epilepsy in humans, multiple genes
may be involved. Another theory suggests that it could be an incomplete form of LFS, and a third concern is that it possibly
is an autosomal dominant trait. A “dominant” trait means that an affected foal only needs to inherit one copy
of the mutated allele to show clinical signs. An example of a dominant trait is HYPP in American Quarter Horses.
FOR RESEARCH INTO JES:
Aleman, MVZ, PhD, Dipl. ACVIM.
Neuromuscular Disease Laboratory,
University of California
One Shields Avenue
Davis, CA 95616-8744
(530) 752-1170 or +1 (530) 752-7267
ON CEREBALLAR ABIOTROPHY RESEARCH. SEPTEMBER 2008. INDIRECT DIAGNOSTIC GENE TEST NOW AVAILABLE.
Research on Cerebellar
Abiotrophy has been ongoing since the mid 1960s by geneticists at the Universities of Cornell, Michigan, Iowa and UC Davis
in the USA and the Universities of Bern and Zurich in Switzerland, of Ghent in Belgium, of Cordoba in Spain, and in Australia
by Professors Dr. J D Baird and Dr. C D Mackensie.
In August 2007 it was announced that locus of the mutant allele
had been located. This was a major breakthrough.
Now Dr. Cecilia Penedo from UC Davis has identified the chromosomal
region which harbors the causative mutation and is continuing with her work in analyzing the genes within this region. She
and her team of researchers have sufficient "markers" in their database and with their knowledge of carrier lineage are offering
an indirect diagnostic test as to the status of the presence of Cerebellar Abiotrophy (CA) in Arabian horses. This test, using
hair root samples, may be requested direct from the laboratory by owners or breeders who feel the need for this test on their
stock. Sufficient DNA is extracted from hair root samples to help establish carrier status.
Initially offering a free
service, the overwhelming response necessitated implementing a fee of $50 USD to offset laboratory costs by March 2008, as
the process is extremely costly. In August 2008, the newly formed Arabian Horse Foundation in USA contributed a $5,000 gift
to the UC Davis Veterinary Genetics Laboratory from their donors for use on further research on Cerebellar Abiotrophy. This
generous donation and any further gifts will aid tremendously in diminishing or eliminating this neurological problem in breeding
herds as long as two carriers are not bred together.
For those who wish to know if their horses are carriers or not
, please send a request to Cecilia Penedo at firstname.lastname@example.org with full name, registration number if applicable and parentage of each individual horse. Providing a full pedigree will
facilitate matters and assure a more speedy response. All requests are treated in the strictest confidence.
wish to contribute Hair Follicle samples at the same time, include the date sent in your email and ship them by airmail to:
– CA, Veterinary Genetics Laboratory
FOAL SYNDROME. MORE GOOD NEWS:
The University of Cornell has reopened their research on Lavender Foal Syndrome. For
further information on sending in samples please contact (note new email address):
Dr. Doug Antczak
James A. Baker
Institute for Animal Health
Veterinary Medicine, Cornell University
The WAHO Office
like to thank Lisa Goodwin-Campiglio, Life Member WAHO, SZED Spanish Arabians, Mallorca, Spain, who contributed this article
and who has been campaigning tirelessly to raise awareness of the research into genetic disorders in Arabians, especially
Newbarn Farmhouse, Forthampton
Gloucestershire GL19 4QD, United Kingdom
+44 (0) 1684 274455
Fax: +44 (0) 1684 274422