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Epilepsy in horses: Aetiological classification and predictive factors. Equine Veterinary Journal, 2012. M. Mayes
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Mar 7, 2017 Generalized myoclonic epilepsy with photosensitivity in juvenile Epilepsy is the most common chronic neurological disease in dogs (3). A study finds that giant pandas roll in horse manure to increase their cold tol
However, most people with JME do not have abnormal results on testing for specific epilepsy genes. About half (50 to 60%) of families with juvenile myoclonic epilepsy report seizures in either a direct relative or a cousin. Juvenile epilepsy is a specific type of epilepsy that develops in young dogs rather than adult and mature dogs, which is much more common. This type of epilepsy is rather rarer than classical types of epilepsy, and has been identified as a breed-specific health issue within the Lagotto Romagnolo dog breed, within which the condition affects a EPIDEMIOLOGY.
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Juvenile idiopathic epilepsy (JIE) in Arabian foals resembles benign-familial neonatal convulsion (BFNC) syndrome, a rare idiopathic epilepsy of new-born humans. BFNC syndrome exhibits genetic heterogeneity, as has been hypothesised to occur in Arabian foals, and is known to be caused by mutations in the voltage-gated potassium channel subunit KCNQ2 and KCNQ3 genes. Juvenile idiopathic epilepsy (JIE) is an inherited disease characterized by recurrent seizures during the first year of life in Egyptian Arabian horses.
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Juvenile idiopathic epilepsy (JIE) is an inherited disease characterized by recurrent seizures during the first year of life in Egyptian Arabian horses. Recurrent seizures can lead to complications, including head injury and aspiration pneumonia. After the first year of life, seizure activity ceases [1].
Identifying genetic causes will help to improve strategic breeding programs.
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Juvenile idiopathic epilepsy (JIE) in Arabian foals resembles benign-familial neonatal convulsion (BFNC) syndrome, a rare idiopathic epilepsy of new-born humans. BFNC syndrome exhibits genetic heterogeneity, as has been hypothesised to occur in Arabian foals, and is known to be caused by mutations in the voltage-gated potassium channel subunit KCNQ2 and KCNQ3 genes.
However, most people with JME do not have abnormal results on testing for specific epilepsy genes. About half (50 to 60%) of families with juvenile myoclonic epilepsy report seizures in either a direct relative or a cousin. Juvenile epilepsy is a specific type of epilepsy that develops in young dogs rather than adult and mature dogs, which is much more common. This type of epilepsy is rather rarer than classical types of epilepsy, and has been identified as a breed-specific health issue within the Lagotto Romagnolo dog breed, within which the condition affects a EPIDEMIOLOGY. Juvenile idiopathic epilepsy has been described in Arabian foals of Egyptian lineage.
Epilepsy is relatively uncommon in horses compared with other species and as yet little information is available. This condition is not usually fatal and appears to be self-limiting Affected foals are born normal and appear normal between epileptic seizures, usually outgrowing the condition between 12 and 18 months.
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