Audiogenic reflex seizures in cats
Open Access
- 27 April 2015
- journal article
- research article
- Published by SAGE Publications in Journal of Feline Medicine and Surgery
- Vol. 18 (4) , 328-336
Abstract
Objectives: This study aimed to characterise feline audiogenic reflex seizures (FARS). Methods: An online questionnaire was developed to capture information from owners with cats suffering from FARS. This was collated with the medical records from the primary veterinarian. Ninety-six cats were included. Results: Myoclonic seizures were one of the cardinal signs of this syndrome (90/96), frequently occurring prior to generalised tonic–clonic seizures (GTCSs) in this population. Other features include a late onset (median 15 years) and absence seizures (6/96), with most seizures triggered by high-frequency sounds amid occasional spontaneous seizures (up to 20%). Half the population (48/96) had hearing impairment or were deaf. One-third of cats (35/96) had concurrent diseases, most likely reflecting the age distribution. Birmans were strongly represented (30/96). Levetiracetam gave good seizure control. The course of the epilepsy was non-progressive in the majority (68/96), with an improvement over time in some (23/96). Only 33/96 and 11/90 owners, respectively, felt the GTCSs and myoclonic seizures affected their cat’s quality of life (QoL). Despite this, many owners (50/96) reported a slow decline in their cat’s health, becoming less responsive (43/50), not jumping (41/50), becoming uncoordinated or weak in the pelvic limbs (24/50) and exhibiting dramatic weight loss (39/50). These signs were exclusively reported in cats experiencing seizures for >2 years, with 42/50 owners stating these signs affected their cat’s QoL. Conclusions and relevance: In gathering data on audiogenic seizures in cats, we have identified a new epilepsy syndrome named FARS with a geriatric onset. Further studies are warranted to investigate potential genetic predispositions to this condition.Keywords
This publication has 49 references indexed in Scilit:
- Characterization of Neuronal Ceroid-Lipofuscinosis in 3 CatsVeterinary Pathology, 2013
- LGI Proteins in the Nervous SystemASN Neuro, 2013
- LGI2 Truncation Causes a Remitting Focal Epilepsy in DogsPLOS Genetics, 2011
- A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriersNeurobiology of Disease, 2011
- Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and humanNature Communications, 2011
- A Missense Mutation in Canine CLN6 in an Australian Shepherd with Neuronal Ceroid LipofuscinosisBioMed Research International, 2010
- A canine Arylsulfatase G ( ARSG ) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosisProceedings of the National Academy of Sciences, 2010
- A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a DachshundMolecular Genetics and Metabolism, 2010
- A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosisBiochemical and Biophysical Research Communications, 2005
- Audiogenic seizures in Wistar rats before and after repeated auditory stimuli: clinical, pharmacological, and electroencephalographic studiesJournal of Neural Transmission, 1988