Peer-reviewed veterinary case report
Episodes of sudden movement problems linked to hyperthyroidism in 7
By Espinosa, Javier et al.·Published in Journal of veterinary internal medicine·2026·Neurology and Neurosurgery Service, United Kingdom·View original on PubMed →
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Original publication title: Paroxysmal dyskinesia associated with hyperthyroidism in 7 cats: a novel manifestation of a metabolic encephalopathy.
- Species:
- cat
Plain-English summary
Seven cats were brought in for episodes of unusual movements, known as paroxysmal dyskinesia, which were linked to hyperthyroidism (HT). The cats showed no signs of neurological issues between episodes, and tests like brain MRIs and EEGs ruled out other conditions. After treating the hyperthyroidism, all the cats experienced a complete stop of the dyskinesia episodes, confirming that managing the thyroid condition resolved the problem. This suggests that if your cat has similar movement issues, hyperthyroidism could be a possible cause.
People also search for: cat unusual movements · hyperthyroidism in cats treatment · paroxysmal dyskinesia in cats
Abstract
BACKGROUND: Paroxysmal dyskinesia associated with hyperthyroidism (HT) is a well-described disorder in humans and has not been previously reported in cats. HYPOTHESIS/OBJECTIVES: Paroxysmal dyskinesia might develop as a consequence of HT in cats, with improvement or cessation of the episodes once normal thyroid function is restored. ANIMALS: Seven client-owned cats. METHODS: Multicenter retrospective observational study comprising cats with clinical signs consistent with the clinical phenotype of paroxysmal dyskinesia based on video recordings, and a concurrent diagnosis of HT. Follow-up information was obtained by contacting referring veterinarians and owners. RESULTS: Seven cats were included. No signs of neurological disease were observed between the episodes except for plantigradism in one cat. Brain MRI studies were performed in 2 cats, revealing no intracranial abnormalities. In 1 cat, a 2-h video-assisted wireless electroencephalography confirmed the absence of epileptic activity. Clinical signs associated with HT were noted in all but 1 cat. After treatment for HT, complete remission of paroxysmal dyskinesia episodes was achieved in all cases, with euthyroid state confirmed in 6 cats. CONCLUSIONS AND CLINICAL IMPORTANCE: HT should be considered a differential diagnosis in cats with paroxysmal dyskinesia, even in the absence of other suggestive signs. Similar to the analogous disorder in humans, the prognosis appears excellent once appropriate treatment for HT is initiated.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/41742482/