O que significa “Limpar”?
O animal não carrega a mutação. Não desenvolverá a doença e não vai passar adiante.
The DNA test for Spongy Degeneration With Cerebellar Ataxia Type 2 (SDCA2) in dogs is essential for early detection of this hereditary neurological disorder. SDCA2 causes progressive loss of coordination and motor skills, severely impacting affected dogs' quality of life. By using this genetic test, breeders can identify carriers and avoid breeding affected puppies, promoting healthier bloodlines. Early diagnosis through DNA testing helps veterinarians manage symptoms more effectively. This test is crucial for breeds prone to SDCA2, ensuring responsible breeding practices. Protect your dog’s future by opting for the SDCA2 DNA test today. Reliable genetic screening supports canine health and longevity.
Spongy Degeneration With Cerebellar Ataxia Type 2 (SDCA2) is a genetic disorder affecting dogs, characterized by progressive loss of coordination and motor skills. A DNA test can identify carriers and affected dogs by detecting mutations responsible for this condition. Early diagnosis through testing helps breeders make informed decisions to reduce the incidence of SDCA2. This test is essential for maintaining the health and quality of affected breeds. Regular screening supports responsible breeding and improves overall canine welfare.
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 →Spongy Degeneration With Cerebellar Ataxia Type 2 (SDCA2) is a genetic neurological disorder that affects dogs, leading to progressive deterioration of the cerebellum and associated structures in the brain. This condition is characterized by the degeneration of nerve cells, which results in a range of motor and coordination issues. The cerebellum plays a crucial role in balance, coordination, and fine motor control, and its impairment can severely affect a dog's daily activities.
Dogs suffering from SDCA2 exhibit various symptoms that often become apparent in early to middle adulthood. Common clinical signs include unsteady gait, difficulty in performing coordinated movements, and an overall lack of balance. Affected dogs may also show signs of tremors, difficulty in standing or walking, and an increased tendency to fall. These symptoms can progressively worsen over time, leading to significant mobility challenges.
SDCA2 is caused by mutations in specific genes responsible for neuronal function and maintenance. The condition is inherited in an autosomal recessive manner, meaning that both parents must carry the gene mutation for an offspring to be affected. The identification of these genetic mutations through DNA testing allows for a better understanding of the disease's mechanism and aids in the development of potential therapeutic strategies.
The diagnosis of SDCA2 is primarily based on clinical observations and can be confirmed through genetic testing. Veterinary neurologists may also perform neurological examinations, imaging studies, and other diagnostic tests to rule out similar conditions and confirm the presence of cerebellar ataxia. Early diagnosis is crucial for managing symptoms and improving the quality of life for affected dogs.
Currently, there is no cure for SDCA2, and management typically focuses on alleviating symptoms and improving the affected dog's quality of life. Supportive care may include physical therapy, nutritional support, and modifications to the dog's environment to ensure safety. In some cases, medications may be prescribed to manage specific symptoms, such as tremors or anxiety. Ongoing research into gene therapy and other innovative treatments holds promise for the future management of this condition.
Spongy Degeneration With Cerebellar Ataxia Type 2 (SDCA2) poses significant challenges for affected dogs and their owners. Understanding the genetic basis, clinical signs, and management options for this condition is essential for effective care. As research progresses, advancements in veterinary medicine may provide new avenues for treatment and support for dogs suffering from this debilitating disorder.
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 Spongy Degeneration With Cerebellar Ataxia Type 2 (SDCA2) 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 ATP1B2 c.130_131ins[LT796559.1:g.50_276].
Não necessariamente. A interpretação depende do padrão de herança e do genótipo resultante.
Mauri Nico, Kleiter Miriam, Dietschi Elisabeth, Leschnik Michael, Högler Sandra, Wiedmer Michaela, Dietrich Joëlle, Henke Diana, Steffen Frank, Schuller Simone, Gurtner Corinne, StokarRegenscheit Nadine, O'Toole Donal, Bilzer Thomas, Herden Christiane, Oevermann Anna, Jagannathan Vidhya, Leeb Tosso. A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). G3 (Bethesda). 2017 Aug 7;7(8):2729-2737. doi: 10.1534/g3.117.043018.
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