Ceroid Lipofuscinosis in The Border
Collie
By Judy DeJong
Information to assist owners and breeders
Ceroid Lipofuscinosis (C.L.) in the Border Collie is a rare disease which affects the nerve cells of
the body. It is also known as Storage Disease.
It is an inherited disease. It is not contagious.
Recent DNA research (November 1995) has identified the gene for the
identical disease which occurs in humans, and is known as Batten's Disease.
Once this gene is identified in Border Collies, we will be able to eliminate
the disease from the breed in one or two generations.
In
The Border Collie Club of NSW Inc. has established a sub-committee
to investigate the incidence of the disease in the breed. Notified cases are
recorded and information is shared with sister Border Collie
clubs.
The names of proven identified carriers and their pedigrees have
been published (with permission from the owners of the animals) to improve the
knowledge of inheritance.
C.L. has been found overseas in other breeds of dogs (Salukis,
English Setters, Cocker Spaniels, Dachshunds), in
Donations from the Club are made to a DNA research programme at the
The Veterinary Clinical Centre at the
Affected dogs do not display any signs until aged approx. 15 to 18 months
and owners of animals with suspect symptoms are asked to contact the Club.
The likelihood of a Border Collie
developing the disease is very small whatever its ancestry and carrier dogs are
not themselves affected in any way. They can be kept as non-breeding pets as in
other aspects they are normal healthy animals.
The occurrence of C.L. in Border Collies is not the fault of any
one person or group. The carrier gene was probably present in a dog imported at
a time when the disease had not been diagnosed. For many years the disease lay
dormant or occurred sporadically & has surfaced now as a breed problem
which we must try to control.
Clinical Signs and Diagnosis of
C.L.
(Storage Disease)
Affected animals appear normal until aged approximately 18 months.
However, from the embryonic stage, there is a metabolic defect which allows a
waste product 'ceroid lipofuscin'
to accumulate in body cells.
The brain cells have very little room for waste products and
symptoms emerge when an accumulation of waste begins to compress and destroy
healthy brain cells. As a result, by 18 months of age some or all of the
following signs may be noted:
Unreasonable apprehension or
fear of familiar objects/surroundings, sight disturbance.
Abnormal gait - is unsteady on feet, has difficulty with jumping or
climbing or placing feet, tends to prop or goose-step.
Demented behaviour, mania,
hyperactivity, rage.
The disease progresses rapidly once the initial signs appear and
the distressed animals have not been kept past the age of 2 1/2 years.
Unfortunately there is no treatment for an affected animal.
To date there is no test available to identify which dogs have
inherited the disease or are carriers of the defective gene. Suspected cases
can be confirmed by brain biopsy. A post mortem examination will give an
accurate diagnosis.
Veterinary Aspects &
Inheritance of C.L.
Ceroid Lipofuscinosis is one of a group of
Metabolic Storage Diseases. It is characterised by the accumulation of ceroid lipofuscin, a wax-like
liquid waste product of cell metabolism which is normally removed by body
enzymes. In cases of C.L. one of the enzymes is missing.
Current research has determined that C.L. has an autosomal recessive mode of inheritance, ie:
Ø
Both male and female are equally
susceptible.
Ø
Sire and dam of an affected dog
must be either carriers or affected themselves.
Ø
Mating a carrier animal to a
clear (non-carrier) animal can produce carrier offspring.
Control
Guidelines are being set for breeders to avoid using PROVEN carrier
animals except for research.
Suspected Cases can be referred
to:
Werribee Victoria
Australia
Phone (03) 741 3500.
Updated information is published in the Club Newsletters to assist members
and to maintain awareness of research developments.
Financial support is essential to the research program and breeders
are asked to make donations to the Fighting Fund from sales or from stud fees.
History
Early this century, F.E. Batten studied and described the disease
in children, hence the name Battens Disease. This is the same disease now being
diagnosed in dogs and known as Ceroid Lipofuscinosis. It is hoped research being conducted on the
disease in dogs will benefit the children suffering from Battens Disease. As in
dogs, there is no cure and no treatment yet available. The life span of
children with Battens Disease is approximately 7 years.
In June 1980, a 17 month old Border Collie
bitch was referred to the
Cases from 3 separate litters were diagnosed in 1985/86 and others
were discovered in 87/88. Since then 6 other litters have been found to have
affected animals, in all (from 1980 to 1996) a total of 15 litters are
diagnosed as having produced C.L.
The Border Collie Club of
The Border Collie Club of NSW Inc. has also formed a sub-committee
which acts in conjunction with the Victorian Club to verify disease related
information. All Border Collie Clubs in
|
Proven Carriers to April 1996 |
|
|
Carrier Dogs |
Carrier Bitches |
|
Ch Bundaliere
Jazz Amatazz C.D |
Blackbeck Black Mystic |
|
Ch Byrnbala
Rhyl Solette |
Crestvale Bonnie Lass C.D. |
|
Ch Crestvale
Gay Roger C.D.X. |
Ch Crestvale
Gay Serena |
|
Ch Finestyle
Sundancer |
Crestvale Natasha |
|
Ch Gotrah
Lancelot Lad CDX |
Finestyle Fancy Free |
|
Ch Kennoway
Bill Bailey |
|
|
Ch Margian
Skipper Too |
Kelsey Lady in Blue |
|
Milangimbi Bronzed Gizmo |
Kennoway Our Wee Maggie |
|
Rosebrook Shar Moss |
Liric Opal Jayde |
|
Tullaview Sono Spade |
Marglo Blue Rhapsody |
|
A/NZ C h Tullaview
Trailblazer |
Monsalvat Amazing Grace |
|
Wallanguma Jock |
Rantara Shantelle Lace |
|
Ch Werlak
Beau Jade |
Rosebrook Corindi |
|
|
Ch Tullacrest
Town Tart |
|
|
Ch Tullaview
Temptress |
Genetic Inheritance of C.L.
Genetically the dog/bitch falls into one of three categories:

Ø
CLEAR: Has not inherited a
defective gene.
Ø
CARRIER: Has inherited the
defective gene from a parent.
Ø
AFFECTED: Has inherited the
defective gene from both parents and has or will develop the disease.
Important points to remember are:
Ø
All progeny of affected animals
must be either carriers or affected.
Ø
To produce an affected animal
both parents must be either carriers or affected.
The Border Collie Club of NSW Inc gratefully acknowledges the
Border Collie Club of
Further information can be
provided by the Border Collie Club of NSW, Inc Sub-committee.
Sub-committee members are:
Ø
Karen Galbraith 02 9607 6364
Ø
Judy de Jong
02 9876 3926
Ø
Bettie Miller 02 9804 7602
Ø
Gail Van Look 02 9823 2462
Ø
Email: Judy de Jong at wild@zeta.org.au
Copyright 2001 Judy de Jong.
wild@zeta.org.au . All rights reserved. You may freely use this article exactly as it
appears here and in its entirety. It may be distributed widely without
permission of the original authors. However, modification or use of portions of
this article must be done so only with the express permission of Judy de Jong or The Border Collie Club of NSW, Inc.
Editor’s Note:
The Border Collie Club of NSW, Inc. is to be congratulated for freely
making others aware of affected pedigrees.
It is only through the sharing of such important information by breeders
and owners with enough responsibility, courage and conviction that such
diseases will be eradicated.