
Cerebellar Abiotrophy in the Scottish
Terrier
Why is my Scottie so wobbly?
What is Cerebellar Abiotrophy?
Cerebellar Abiotrophy (CA) is a neurological disease
recently described in the Scottish Terrier. The term defines
progressive, premature cell death in the cerebellum, an area
of the brain that controls smooth, coordinated motor skills
such as walking. If the cerebellum is damaged or begins to
degenerate, fine tuned, precise movement is affected and
smooth, voluntary movements become coarse, jerky and
uncoordinated. Simply put, a dog affected with CA becomes
ataxic, or wobbly.
What are the symptoms of CA?
Dogs affected with CA will slowly lose their well-defined
motor skills and may exhibit subtle incoordination or
clumsiness. An owner might observe an unsteady gait, a loose
and wobbly rear end or noticeable rolling of the hips.
Affected dogs can trip occasionally, bang their chin, fall
down, or have trouble negotiating stairs. Eventually, they
may begin using the nose to aid in balance and develop a
wide-based stance in the rear legs. Irregularities in the
front legs can also be present. The symptoms may become
severe in one affected dog or remain relatively mild in
another. There might be a faster rate of degeneration in one
dog or very slow progression of the disease in another, with
gradual changes taking place over several years.
Can CA be difficult to diagnose?
Yes. At this time there is no test to definitively
diagnose CA in the living animal. A clinical diagnosis is
made based on symptoms, but a final diagnosis can only be
made with a post mortem exam. Symptoms of CA can be confused
with those of Scottie Cramp, another genetic disorder known
to exist in the breed. However, Cramp is an occasional
condition, brought on by stress, excitement and/or exercise.
Most of the time, a Scottie with Cramp will appear perfectly
normal. By contrast, the incoordination associated with CA
is always present once its been detected. Patellar luxation
(slipping knee caps) can also occur in Scotties, but this is
a separate, unrelated condition.
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Are CA symptoms present at birth?
No. Affected dogs seem normal at birth. Occasionally
symptoms are seen as early as 6 months of age, but many
times they aren't noticed until the dog is one year or
older.
Is CA a fatal disease?
No. Affected dogs can live out a full lifespan. The
disease affects only balance and motor skills; the mind
remains normal throughout the disease process.
What is the quality of life one can expect in a dog
affected with CA?
Affected dogs can have a good quality of life. The
disease is very slow to progress and the dog is able to
play, enjoy life and participate in the lifestyle his/she is
accustomed to for some time. It's been said that the disease
is harder on the owner than it is on the dog. One has to
keep in mind that CA is not painful. However, some Scotties
with advanced CA may require assistance while walking,
eating and drinking.
Is CA a hereditary disease?
Yes. CA is caused by a simple autosomal recessive gene.
Affected dogs have 2 copies of the defective gene, one
inherited from each parent. Therefore, both parents of an
identified affected dog are known carriers of CA. Full
siblings may be affected, they may be carriers or they may
be clear. Males and females can be affected.
Is there any treatment available for CA?
No. Unfortunately, there is none available at this time.
Some owners have tried vitamins, dietary supplements and
acupuncture, hoping to delay the progression of the disease.
There is no medical data supporting benefit from any of
these treatments, but that is an issue to be discussed with
a qualified veterinarian.
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What is being done about CA in the
Scottie?
The STCA HTF is fully involved and is looking into CA in
the Scottish Terrier. In 1995, the STCA HTF Breed Survey
indicated that the incidence of ataxia in Scotties was a re-
ported 13%. It is not possible to know how many of these
cases were indeed CA, but the incidence of ataxia was
relatively high. In 2001, the STCA HTF retained the services
of Dr. Jerold Bell DVM, Assistant Professor of Genetics at
Tufts University, to look into this matter. Dr. Bell is
currently accepting information about any Scottie with
possible neurological disease. He will assist owners by
determining a diagnosis, which may or may not turn out to be
CA. Once he collects enough data, Dr. Bell's goal is to
determine how widespread CA is in the breed and to make
recommendations on how to help lower the incidence of this
disease. Eventually Dr. Bell, other doctors and research
scientists hope to prevent CA from occurring in the future.
One goal is to conduct DNA studies, which may one day
provide a test for breeders to identify carriers in their
lines. Dr Bell needs your help.
Dr. Jerold Bell asks that those who have a dog
they suspect may have CA contact him. He will review a video
and a pedigree (if available) of your Scottie to determine
if he or she could be affected and offer a diagnosis. There
is no charge for this service. Dr. Bell offers complete
confidentiality.
Dr. Alexander de Lahunta, a renowned neurologist,
is assisting Dr. Bell in this research. He has offered to do
necropsies (post mortem exams) on deceased Scotties affected
with CA to confirm the diagnosis at no cost. He will also
accept and review a video of a Scottie suspected of having
CA.
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Contacts
If you suspect you have a Scottie with CA and are
uncertain what the symptoms might look like, a video is
available showing multiple Scotties at different stages of
the disease. Please make your request for a copy of this
video to:
Debbie Smith
STCA CA Research Project Chairman
6556 Pinar Road Harborcreek, PA 16421
(814) 899-2856
E-mail:
LITLBLKDOG@aol.com
For Diagnostic Information, contact:
Dr. Jerold Bell, DVM
Veterinary Genetic Counseling
PO Box 3399
Enfield, CT 06083
E-mail:
Geneticvet@aol.com
Dr. Alexander de Lahunta, DVM
Dept of Biomedical Sciences
College of Veterinary Medicine
Cornell University
Ithaca, NY 14853
E-mail:
AD43@comell.edu
Copyright 2004
Scottish Terrier Club of America
Health Trust Fund
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