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Neurocognitive Disorder Analysis

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The term ‘neurocognitive disorder’ was recently established by the DSM-V and is divided into major neurocognitive disorders and mild neurocognitive disorders. The DSM-V has grouped the terms ‘delirium, dementia, and amnestic and other cognitive disorders’ that were previously used in the DSM-IV-TR into one term known as ‘neurocognitive disorders’ (Mcanulty, 2013). Major neurocognitive disorder consisted of the term dementia in the DSM-IV-TR while minor neurocognitive disorder was a diagnosis not previously included in the DSM. Major neurocognitive disorders will affect an individual's everyday life significantly, while a mild neurocognitive disorder may not. Neurocognitive disorders primarily affect an individual’s cognitive abilities acquired …show more content…

Neurocognitive disorders can occur at any stage in life and may be caused by a variety of factors. Progressive forms of major neurocognitive disease include Alzheimer’s disease, vascular dementia, frontotemporal lobar degeneration, and Lewy body disease. Progressive forms of neurocognitive disease usually occur by genetics, protein plaque buildup in the brain, fibrous tangles in the brain, blocked blood vessels to the brain, or a breakdown of nerve cells in the frontal and parietal lobes of the brain. Alzheimer’s disease is the most prevalent progressive neurocognitive disorder and results in a slow decline in cognitive functioning mainly affecting the areas of the brain controlling “memory, language, judgment and spatial recognition” (Mayo Clinic …show more content…

Individuals with this diagnosis can also experience rapid eye movement (REM) sleep behavior disorder which includes acting out dreams while in a sleep state. Frontotemporal lobar degeneration occurs in individuals ages 50-70 and results in “inappropriate behaviors, language impairments, trouble with cognition involving thinking and concentration, as well as movement impairments” (Mayo Clinic, 2015). Other forms of neurocognitive disorders include trauma, traumatic brain injury, Parkinson’s disease, and Huntington’s disease (Grohol, 2015). Huntington’s disease is a genetic disorder that affects specific nerve cells in the brain and spinal cord. This disease occurs in earlier years, typically between the ages of 30-40 and symptoms include “changes in personality including anxiety and irritability, a severe decline in cognition, and weakness affecting gait” (Swierzerski, 2014). Traumatic brain injuries occur from some form of head trauma and symptoms are determined by the part of the brain that’s affected but can include “difficulty coordinating movements, problems with speech, and/or memory impairments”. Individuals with a diagnosis of Parkinson’s disease can also often times also develop symptoms of dementia in addition to tremor symptoms

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