(^56) 5. 3. 4. 2.^ refiprogress more rapidly, and there is an earlier appearance now enable clinicians to use specifibody disease is fairly similar to AD; however, it tends to tify the disease at an accuracy rate of 70% to 90% (Bourgeois, Seaman, & Servis, 2008).cerebral cortex and brainstem (Andreasen & Black, 2006). Va sc u la rDementia Due to Lewy Body Disease. Lewy bodies—eosinophilic inclusion bodies—seen in the traumatic brain injury.signifitoms associated with dementia can be brought on by a equivalent of small strokes caused by arterial hypertension or cerebral emboli or thrombi, which destroy many areas of the brain. The onset of symptoms is more abrupt than in et al., 2006). This disorder is distinctive by the presence of rather than as a gradual deterioration.of visual hallucinations and parkinsonian features (Rabins, Dementia Due to HIV DiseaseDementia Due to Head Traumaassociated with human immunodefiby biopsy or autopsy examination of brain tissue, although ease can lead to brain infections by other organisms. HIV also appears to cause dementia directly.AD and runs a highly variable course, progressing in steps ●^ nement of diagnostic criteria and new diagnostic tools ALTERATIONS IN PSYCHOSOCIAL ADAPTATION cant cerebrovascular disease. The client suffers the Dementia. This type of dementia is caused by. The immune dysfunction c clinical features to iden-. The syndrome of symp- ciency virus (HIV) dis-Clinically, Lewy
2 2506_Ch03_054-070.indd 56 506 Ch 03 054 - 070 .ind 6. 7. 9. 8. d 56 Dementia Due to Creutzfeldt-Jakob Disease. disease is often misdiagnosed as AD.Symptoms are strikingly similar to those of AD, and Pick’s atrophy in the frontal and temporal lobes of the brain. onset.Dementia Due to Pick’s Disease. study, the median duration of the disease was 21.4 years.Dementia Due to Parkinson’s Disease. ents have the shortest duration (Foroud et al., 1999). In this One study concluded that juvenile-onset and late-onset cli-The average duration of the disease is based on age at onset. curs in the areas of the basal ganglia and the cerebral cortex. transmitted as a Mendelian dominant gene, and damage oc-“slow virus” or prion. The clinical presentation is typical of Dementia Due to Huntington’s Disease. with Parkinson’s disease closely resemble those of AD.of the basal ganglia. The symptoms of dementia associated ease is caused by a loss of ner ve cells in t he substant ia nigra of dementia is caused by a transmissible agent known as a the syndrome of dementia, and the course is extremely rapid, with progressive deterioration and death within 1 year after Pathology occurs from Parkinson’s dis-This disease is This form 1 10/1/10 9:33:38 AM 0 / 1 / 10 9 : 33 : 38 AM
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