狗 凱利藍梗犬多系統退化（CMSD-KBT）

依品種或臨床分類過濾 DNA 測試

The Canine Multiple System Degeneration (CMSD) DNA test is essential for Kerry Blue Terrier owners to ensure their dogs' health. CMSD is a hereditary neurological disorder affecting coordination and movement in Kerry Blue Terriers. Early genetic testing helps identify carriers and affected dogs, enabling responsible breeding decisions. By using the CMSD DNA test, breeders can reduce the risk of passing this debilitating condition to future generations. This test provides accurate, reliable results, promoting the well-being of your Kerry Blue Terrier. Protect your dog’s health with the CMSD DNA test today. Regular screening supports a healthier, happier canine companion.

縮寫 ： CMSD-KBT

分析突變： SERAC1 c.1536G>A

繼承： 體染色體隱性遺傳

可從包裝中取得： Basic

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Understanding Canine Multiple System Degeneration in Kerry Blue Terriers (CMSD-KBT)

Canine Multiple System Degeneration (CMSD) is a progressive neurological disorder that primarily affects Kerry Blue Terriers. This condition is characterized by the degeneration of multiple systems within the nervous system, leading to a range of debilitating symptoms that can significantly impact the quality of life of affected dogs.

Symptoms of CMSD-KBT

The symptoms of CMSD-KBT typically manifest in early to mid-adulthood, although the age of onset can vary. Common signs include balance problems, difficulty walking, and a general lack of coordination. As the disease progresses, affected dogs may exhibit muscle weakness, tremors, and a decline in overall mobility. In some cases, dogs may also experience changes in behavior, such as increased anxiety or a reluctance to engage in normal activities.

Pathophysiology of CMSD-KBT

The underlying cause of CMSD-KBT lies in genetic mutations that affect the nervous system's ability to function properly. These mutations lead to the degeneration of nerve cells, which in turn causes a breakdown of communication between the brain and the body. This disruption results in the clinical symptoms observed in affected dogs. Understanding the genetic basis of CMSD-KBT is crucial for breeders and owners, as it allows for informed decisions regarding breeding practices and the management of affected animals.

Management and Care for Affected Dogs

While there is currently no cure for CMSD-KBT, management strategies can help improve the quality of life for affected dogs. Regular veterinary check-ups are essential for monitoring the progression of the disease and addressing any health concerns that arise. Physical therapy and rehabilitation exercises can assist in maintaining mobility and strength. Additionally, providing a safe and supportive environment can help dogs cope with their symptoms and enhance their overall well-being.

結論

Canine Multiple System Degeneration in Kerry Blue Terriers is a serious condition that requires attention from dog owners and breeders. By understanding the symptoms, underlying causes, and management strategies associated with CMSD-KBT, stakeholders can work towards improving the lives of affected dogs while making informed breeding decisions to reduce the prevalence of this condition in the breed.

被認可參加測試的品種： 凱利藍梗犬多系統退化（CMSD-KBT）

• Kerry Blue Terrier

🧬 Interpretation of genotypes CMSD-KBT

❓ 了解有關基因型解釋的更多信息

常見問題：理解解釋

「清晰」是什麼意思？

該動物不攜帶突變。就不會發展成這種疾病 並且不會傳遞下去。

「航母」是認真的嗎？

不會。該動物通常是健康的，但可以將突變傳播給它的 後代。

如果動物「受到影響」怎麼辦？

它攜帶兩個突變的副本。預計臨床症狀取決於 這種疾病。它不應該被培育。

為什麼男性/女性之間會有差異？

有些疾病與性別有關，因此其表現因性別而異 動物的性別。

預測後代

DNA 測試常見問題解答

這個 DNA 測試檢測到什麼？

This DNA test detects the mutation associated with Canine Multiple System Degeneration In Kerry Blue Terrier (CMSD-KBT) in order to identify clear, carrier, or at-risk animals.

為什麼要測試繁殖動物？

DNA 測試有助於飼養員計劃更安全的交配並降低將突變傳播給後代的風險。

這個測試的​​繼承模式是什麼？

此測試報告的遺傳模式是體染色體隱性遺傳。

此測試分析哪一種突變？

This test analyses the mutation SERAC1 c.1536G>A.

攜帶動物是否必然受到影響？

未必。解釋取決於遺傳模式和產生的基因型。

參考

Johnson GS, Mhlanga-Mutangadura T, Morava E, Kozicz T, Taylor JF, O’Brien DP, Schnabel RD. Canine Multiple System Degeneration is Associated with Distinct SERAC1 Mutations in Two Different Dog Breeds [abstract]. Presented at the 63rd Annual Meeting of the American Society of Human Genetics in Boston, Massachusetts; 2013 Oct 22-26.