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CoGenesis® AD

CoGenesis® AD

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阿茲海默症是最常見的認知障礙形式。根據世衛數據,阿茲海默症佔認知障礙個案的60-70%。

認知障礙症狀會在部份長者身上出現,但不是正常衰老的一部份。其中,有5%的病例屬於早發性阿茲海默症。了解阿茲海默症的基因變異有助評估早發或晚發性阿茲海默症的遺傳風險。

 

根據文獻,約35-60%的早發性阿茲海默症患者擁有家族病史。

Porter, T., Gozt, A.K., Mastaglia, F.L. and Laws, S.M. (2019). The Role of Genetics in Alzheimer's Disease and Parkinson's Disease. In Neurodegeneration and Alzheimer's Disease.

 

若擁有一組APOE4基因變異會比其他患者多2至3倍風險;若擁有兩組該基因變異發病的風險將會增加到10至15倍。

Van Cauwenberghe, C., Van Broeckhoven, C. & Sleegers, K. The genetic landscape of Alzheimer disease: clinical implications and perspectives. Genet Med 18, 421–430 (2016).

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Codex offers hereditary genetic tests for cancer and neuro diseases, and comprehensive genomic profiling for cancer treatments. The services provided by Codex Genetics are for research use only, and they are not suitable for diagnostic and/or treatment use, unless otherwise instructed by licensed medical professionals. 

科德施提供與腦神經退化和癌症基因相關的測試。 除非有醫療專業人員另行指示,此網站的服務只供研究用途,並不供作診斷或治療任何疾病之用。

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