O que significa “Limpar”?
O animal não carrega a mutação. Não desenvolverá a doença e não vai passar adiante.
Unlock the secrets of your Norwegian Buhund’s health with a DNA test for Hereditary Ataxia (HA). This genetic screening is crucial for responsible breeding, helping to identify carriers and reduce the risk of this debilitating condition. By understanding your dog’s genetic makeup, you can make informed decisions to enhance their quality of life. Early detection of HA allows for timely intervention and management strategies. Ensure your Norwegian Buhund thrives by choosing a reliable DNA test today. Protect your furry friend from hereditary conditions and contribute to healthier breeding practices. Invest in your dog’s future with knowledge and proactive care.
Hereditary Ataxia (HA) is a genetic condition affecting Norwegian Buhunds, leading to progressive coordination loss and mobility issues. DNA testing for HA can identify carriers and affected individuals, allowing breeders to make informed decisions to reduce the incidence of the disorder. Early detection through genetic testing can help manage the health and quality of life for these dogs. Responsible breeding practices, informed by DNA results, play a crucial role in preserving the breed's integrity. Ultimately, such testing promotes the welfare of Norwegian Buhunds and supports their longevity.
Este teste de DNA está incluído a partir do nosso pacote Basic - e também faz parte dos packs Basic, Standard, Advanced, Complete.
Ver pacotes de teste de DNA →Hereditary Ataxia (HA) is a neurological condition that affects coordination and balance in dogs, specifically noted in the Norwegian Buhund breed. This condition is characterized by the degeneration of the cerebellum, which is responsible for motor control. Affected dogs may exhibit symptoms such as unsteady gait, difficulty in performing tasks, and an overall lack of coordination.
The symptoms of Hereditary Ataxia typically become apparent in young dogs, usually between six months and three years of age. Common signs include stumbling, swaying, and difficulty in walking or running. Affected dogs may also display abnormal head movements or postures, as well as a reduced ability to judge distances, which can lead to accidents or falls.
Hereditary Ataxia is caused by a genetic mutation that affects the development and function of the nervous system. This condition is inherited in an autosomal recessive manner, meaning that both parents must carry the gene mutation for the offspring to be affected. A dog that inherits only one copy of the mutated gene will be a carrier but will typically remain healthy.
DNA testing for Hereditary Ataxia is crucial for breeders and pet owners. By identifying carriers of the gene mutation, breeders can make informed decisions to prevent the propagation of this condition. Responsible breeding practices can significantly reduce the incidence of Hereditary Ataxia in future generations of Norwegian Buhunds. For pet owners, testing can provide insights into their dog's genetic health, enabling proactive management of any potential health issues.
While there is currently no cure for Hereditary Ataxia, management strategies can help improve the quality of life for affected dogs. This may include physical therapy to enhance mobility and coordination, as well as modifications to the home environment to ensure safety. Regular veterinary check-ups are essential to monitor the progression of the condition and to address any secondary health concerns that may arise.
Hereditary Ataxia in Norwegian Buhund is a significant condition that can impact the lives of affected dogs and their families. Through genetic testing and responsible breeding practices, the prevalence of this disorder can be minimized, ensuring healthier generations of this beloved breed. Understanding the implications of Hereditary Ataxia is vital for anyone involved with Norwegian Buhunds, from breeders to pet owners.
O animal não carrega a mutação. Não desenvolverá a doença e não vai passar adiante.
Não. O animal é geralmente saudável, mas pode transmitir a mutação ao seu descendência.
Ele carrega duas cópias mutadas. Os sinais clínicos são esperados dependendo a doença. Não deveria ser criado.
Algumas doenças estão ligadas ao sexo, pelo que a sua expressão varia dependendo do sexo do animal.
This DNA test detects the mutation associated with Hereditary Ataxia In Norwegian Buhund (HA) in order to identify clear, carrier, or at-risk animals.
Os testes de DNA ajudam os criadores a planejar acasalamentos mais seguros e a reduzir o risco de transmissão da mutação aos descendentes.
O modo de herança relatado para este teste é Autossômico Recessivo.
This test analyses the mutation KCNIP4 c.436T>C.
Não necessariamente. A interpretação depende do padrão de herança e do genótipo resultante.
Jenkins Christopher A, Kalmar Lajos, Matiasek Kaspar, Mari Lorenzo, Kyöstilä Kaisa, Lohi Hannes, Schofield Ellen C, Mellersh Cathryn S, De Risio Luisa, Ricketts Sally L. Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs. PLoS Genet. 2020 Jan 30;16(1):e1008527. doi: 10.1371/journal.pgen.1008527. eCollection 2020 Jan.
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