Peer-reviewed veterinary case report
Dystonia in dogs and cats - symptoms and treatment
By Santifort, Koen M & Mandigers, Paul J J·Published in Journal of veterinary internal medicine·2022·Evidensia Referral Hospitals, Netherlands·View original on PubMed →
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Original publication title: Dystonia in veterinary neurology.
Plain-English summary
Dystonia is a condition that affects movement in both humans and animals, including dogs and cats. It involves involuntary muscle contractions that can lead to unusual movements or postures. This review looks at how dystonia is defined and diagnosed in pets, as well as its possible causes and treatments. It also highlights the importance of noting specific details when observing a pet with dystonia, such as what they were doing when the symptoms started, how long the symptoms last, and any other related signs. Understanding these factors can help veterinarians better diagnose and treat this condition in pets.
Abstract
Dystonia is a clinical sign and main feature of many movement disorders in humans as well as veterinary species. It is characterized by sustained or intermittent involuntary muscle contractions causing abnormal (often repetitive) movements, postures, or both. This review discusses the terminology and definition of dystonia, its phenomenology, and its pathophysiology, and provides considerations regarding the diagnosis and treatment of dystonia in dogs and cats. In addition, currently recognized or reported disorders in dogs and cats in which dystonia is a particular or main feature are discussed and comparisons are made between disorders featuring dystonia in humans and animals. We suggest that when describing the phenomenology of dogs and cats with dystonia, if possible the following should be included: activity being performed at onset (e.g., resting or running or exercise-induced), body distribution, duration, responsiveness (subjective), severity, temporal pattern (i.e., paroxysmal or persistent, severity at onset and at later stages), presence or absence of autonomic signs (e.g., salivation), presence or absence of preceding signs (e.g., restlessness), presence or absence of signs after dystonia subsides (e.g., sleepiness), coexistence of other movement disorders, any other neurological manifestations, and possible links to administered medications, intoxications or other associated factors. We also suggest that dystonia be classified based on its etiology as either structural genetic, suspected genetic, reactive, or unknown.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/36086931/