Hoof wall separation disease: A Review.
Abstract: Hoof wall separation disease (HWSD) is a genetic defect in Connemara ponies characterised by separation and cracking of the dorsal hoof wall. The disease can result in chronic inflammation, severe lameness and laminitis. Affected ponies typically show clinical signs within the first six months of life. The disease is inherited as an autosomal recessive trait. The genetic mutation is a frameshift mutation in the gene SERPINB11, (c.504_505insC). Carriers are completely normal, only ponies that are homozygous for the mutation will have clinical signs of the disease. Within the Connemara breed, carrier frequency has been estimated at 14.8% and the mutation has not been identified in other breeds at this time. While there is no definitive cure for HWSD, management through targeted hoof care and the use of special shoes may be beneficial. Additionally, environmental management may lessen the severity of clinical disease in affected ponies. Genetic testing of Connemara ponies is required for all new registrations. This review of Hoof wall separation disease (HWSD) in Connemara ponies describes the clinical presentation, histopathologic findings, genetic discovery and resulting DNA test and management considerations for affected ponies.
Publication Date: 2021-07-11 PubMed ID: 36172455PubMed Central: PMC9512258DOI: 10.1111/eve.13530Google Scholar: Lookup
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Summary
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This research reviews Hoof Wall Separation Disease (HWSD), a genetic defect in Connemara ponies that manifests as the separation and cracking of the dorsal hoof wall and can lead to chronic inflammation and lameness. The researchers detail the nature of the disease, its clinical presentation, genetic origins, and recommendations for management of afflicted ponies.
Disease Overview
- The study emphasises on a widespread disease specifically pertaining to Connemara ponies known as Hoof Wall Separation Disease (HWSD). This defect has a genetic origin and manifests itself by causing separation and cracks within the dorsal hoof wall.
- The ailment may result in chronic inflammation, extreme gait abnormality or lameness, and may eventually develop into laminitis, a serious condition affecting the horse’s hoof.
- Warning signs become evident within the first half-year of the pony’s life. Note, however, that the disease is inherited as an autosomal recessive trait. This means a pony needs to inherit copies of the defective gene from both parents to have the disease.
Genetic Aspect
- A particular change in the DNA sequencing has been detected as the cause of this mutation. The precise change is known as a frameshift mutation— specifically, mutation c.504_505insC.
- Carriers —ponies who have just one copy of the defect — do not show any signs of the disease. Only ponies receiving a copy from each parent, thereby making them homozygous for the mutation, will exhibit clinical symptoms.
- According to the research, approximately 14.8% of Connemara ponies carry this mutation, but it is yet to be found in other breeds.
Management and Cure
- There is no definitive cure for HWSD as of now. However, the disease symptoms can be managed effectively through specialised hoof care and the usage of particular hoof shoes.
- Environmental management, such as maintaining the pony in a well-maintained area, could also contribute to reducing the severity of the disease’s clinical presentation.
Genetic Testing
- The research suggests that genetic testing of Connemara ponies should be compulsory for all new registrations to screen for carriers and potentially mitigate the effects of the disease by ensuring carriers are not interbred.
Cite This Article
APA
Finno CJ.
(2021).
Hoof wall separation disease: A Review.
Equine Vet Educ, 34(9), 501-502.
https://doi.org/10.1111/eve.13530 Publication
Researcher Affiliations
- Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA 95616, USA.
Grant Funding
- L40 TR001136 / NCATS NIH HHS
Conflict of Interest Statement
Author’s declaration of interests No conflicts of interest have been declared.
References
This article includes 2 references
- Finno CJ, Stevens C, Young A, Affolter V, Joshi NA, Ramsay S, Bannasch DL. SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies. PLoS genetics 2015;11:e1005122.
- Wolf U. Identical mutations and phenotypic variation. Hum Genet 1997;100:305–321.
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