Laryngeal and pharyngeal dysfunction in horses homozygous for hyperkalemic periodic paralysis.
Abstract: Evaluate histories, clinical signs, and laboratory data of 69 horses homozygous by DNA testing for hyperkalemic periodic paralysis (HPP). Methods: Cohort study. Methods: 69 of 189 horses testing homozygous for HPP between October 1992 and November 1994. Methods: Questionnaires addressing signalment, training regimes, medical history, and current status of affected horses were sent to owners, trainers, or attending veterinarians. Data from completed questionnaires were tabulated and evaluated, using descriptive statistics. Results: Sixty-nine (37%) of 189 questionnaires were completed and returned. Clinical episodes of muscle weakness or paralysis varied in severity and frequency from mild muscle fasciculations to recumbency and death. Sixty-three of 68 HPP-affected horses were reported to have had stridor associated with exercise, excitement, stress, or episodes of muscle paralysis. Common endoscopic findings in affected horses included pharyngeal collapse, pharyngeal edema, laryngopalatal dislocation, and laryngeal paralysis. Twelve of 27 horses receiving acetazolamide had decreases in stridor while receiving medication. Conclusions: Most horses testing homozygous for HPP had clinical signs associated with pharyngeal and laryngeal dysfunction. Hyperkalemic periodic paralysis should be included on a differential list for horses examined for signs of laryngeal or pharyngeal dysfunction or stridor. Treatment with acetazolamide may help to control respiratory tract signs associated with this disease.
Publication Date: 1996-08-15 PubMed ID: 8756883
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigates hyperkalemic periodic paralysis (HPP) in horses, a genetic disorder that affects muscular function, with the goal of understanding its effects on pharyngeal and laryngeal dysfunction. The study consists of a survey of owners, trainers, or veterinarians of horses with HPP, and shows a high occurrence of stridor and other symptoms related to laryngeal or pharyngeal issues in such affected horses.
Study Methodology
- This research was conducted as a cohort study and involved the collection of data from 69 horses that tested homozygous for HPP between October 1992 and November 1994. Homozygous refers to the possession of two identical forms of a particular gene inherited from each parent.
- To gather the data, questionnaires addressing various aspects of the horses’ life such as their medical history, training regimes, physical condition, and current status were sent out to the horse owners, trainers, or attending veterinarians.
- Completed data were then tabulated and evaluated using descriptive statistics.
Study Findings
- Out of the 189 horses that were identified as homozygous for HPP, responses were received from 69 (37%).
- These responses indicated that horses with HPP suffer from a varying degree of muscle weakness or paralysis, which could be mild fasciculations to serious episodes leading to the inability to stand or even death.
- An overwhelming majority (63 out of 68) of the horses with HPP were found to have stridor (a harsh or grating sound during breathing) related to exercise, stress, or during episodes of muscle paralysis.
- The most common endoscopic findings in affected horses were issues related to the pharynx and larynx, such as pharyngeal collapse and edema, laryngopalatal dislocation, and laryngeal paralysis.
- The use of a medication named acetazolamide was noted to decrease the occurrence of stridor in 12 out of 27 horses on this treatment.
Conclusions
- This study concludes that most horses that are homozygous for HPP display clinical signs associated with pharyngeal and laryngeal dysfunction.
- It highlights the importance of considering HPP in the differential diagnosis of horses presented with signs of laryngeal or pharyngeal dysfunction or stridor.
- Furthermore, it suggests that treatment with acetazolamide may help control respiratory symptoms associated with HPP in horses.
Cite This Article
APA
Carr EA, Spier SJ, Kortz GD, Hoffman EP.
(1996).
Laryngeal and pharyngeal dysfunction in horses homozygous for hyperkalemic periodic paralysis.
J Am Vet Med Assoc, 209(4), 798-803.
Publication
Researcher Affiliations
- Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis 95616, USA.
MeSH Terms
- Animals
- Cohort Studies
- Electromyography / veterinary
- Homozygote
- Horse Diseases / genetics
- Horse Diseases / physiopathology
- Horses
- Hyperkalemia / genetics
- Hyperkalemia / physiopathology
- Hyperkalemia / veterinary
- Laryngoscopy / veterinary
- Larynx / physiopathology
- Paralyses, Familial Periodic / genetics
- Paralyses, Familial Periodic / physiopathology
- Paralyses, Familial Periodic / veterinary
- Pharynx / physiopathology
- Point Mutation
- Respiratory Sounds / etiology
- Respiratory Sounds / veterinary
- Sodium Channels / chemistry
- Sodium Channels / genetics
- Surveys and Questionnaires
- Videotape Recording
Citations
This article has been cited 1 times.- Jurkat-Rott K, Lehmann-Horn F. Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis. Neurotherapeutics 2007 Apr;4(2):216-24.
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