Various disorders have discussed under brief descriptions
asfollows:
Cerebellar Abiotrophy (CA)
Synony
Cerebellar cortical abiotrophy (CCA)
‘Common symptoms:
+ In most cases foals appear normal at birth, and
symptoms generally become noticeable after four
months or may be after one year of birth
+ Horses affected with Cerebellar Abiotrophy tend to
startle easily and often fall.
+ Common symptoms include head tremor, a lack of
balance and other neurological issues.
+ Affected horses may develop a wide-based stance of
the forelegs and difficulty ising from a reclining position.
Genetics: Cerebellar Abiotrophy (CA) has a recessive trait
Of inheritance, which means that only horses that carry
two copies of the mutation (CA/CA) will be affected, and
Carrier horses (N/CA) will not develop the disease but may
pass ton to their offspring,
Table 1: Inheritance pattern for Autosomal Recessive trait
(Labokiin, 2007)
Sire Dam | Offspring
clear | x | clear | 100% Clear
clear | x | Carer | Sox Clear + 50% carers
Clear | x | affected | 100% carriers
amir | x | clear — | Sow clear + 50% caries
Camier | x | Carrie | 259% clear + 25% affected +
50% caries *
Carer | x | affected | 50% carers + 50% affected
Affected | x | clear * | 100% carriers
‘Affected | x | Carrier | S05 carers + 50% affected
Affected | x | afected | 100% atected
Carriers have only one copy of the mutation so they do
not express the trai
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+ The mutation can be passed down, sometimes for
several generations, without the trait being expressed
even though the mutation is present in a horse's
genotype.
*+ Both parents must be carriers and each must pass along
copy of the mutation in order for afoal to be affected
Differential diagnosis: Cerebellar Abiotrophy is
sometimes confused with Wobbler's syndrome, Equine
Protozoal Myeloencephalitis and injury-related problems
Prevention and Controll: Cerebellar Abiotrophy can be
prevented by selective breeding approach, This disorders
‘ot curable; however, genetic testing can detect carriers
horse, therefore genetic testing is important to control the
spread of the disease,
Congenital Stationary Night Blindness (CSNB)
Breed affected: Appaloosas breed are mostly affected
Description: Impaired or absent night vision. This
condition makes the horses less visible particularly in low
intensity light. CSNB is a form of non-progressive night
blindness. There is more than one form of CSNB that can
‘occur in horses. There is a common form of CSNB caused
by the TRPMA gene, also known as Leopard Complex,
which causes “appaloosa” patterns, Mutation TRPM1
gene impairs the function of rods in the eyes that allow
animals to see better in the dark. The eye itself is not
affected, but a pathway from the eye to the brain is
impaired, Ifthe horse have night blind since birth, then itis