Alzheimer’s Disease Genetic Mutations: Mini Review
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چکیده
Alzheimer’s disease is one of the least understood brain disorders. The genetic association of Alzheimer’s disease (AD) is an area that attracts the interest of neuroscientists since it is similar to other neurological illnesses but quite a complex disorder. It is considered to be a genetically dichotomous disease exhibiting two currently documented forms known as early onset familial cases that usually characterized by Mendelian inheritance and late onset after age 65, with no consistent mode of transmission [1]. Alzheimer’s disease is an autosomal dominant inheritance disorder. Most families with AD typically develop symptoms between the ages of 30 to 60 years old. The greatest risk factor of Alzheimer’s is age. Genetic predisposition for AD has been in more current times and a topic of interest. The genetic mutations of Alzheimer’s are still being researched and poorly understood; however, early onset Alzheimer’s genetic mutations are better understood.
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تاریخ انتشار 2016