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339 Possible Causes for Progressive Dementia with Onset of Disease

  • Alzheimer Disease

    Dementias characterized at onset by prominent motor signs include dementias with Lewy bodies, idiopathic Parkinson's disease, progressive supranuclear palsy, cortico-basal[ncbi.nlm.nih.gov] Her condition progressed to dementia with behavioral changes. Magnetic resonance imaging showed early left perisylvian and bitemporal atrophy.[ncbi.nlm.nih.gov] Alzheimer's is a progressive disease, where dementia symptoms gradually worsen over a number of years.[alz.org]

  • Hemochromatosis

    dementia.[doi.org] […] extrapyramidal disease, 21 choreoathetoid movements, and parkinsonism.[doi.org] […] when absent, pathological intracellular iron accumulation occurs. 18– 20 Neuroferritinopathy, a recently described autosomal dominant disorder, is characterised by late onset[doi.org]

  • Alcohol Dementia

    Researchers found that 30 people with primary progressive aphasia—a form of early-onset dementia—were significantly worse at identifying and naming celebrities, scoring an[healthline.com] […] knowledge of words and objects," lead study author Tamar Gefen, a doctoral candidate in neuropsychology at Northwestern University's Cognitive Neurology and Alzheimer's Disease[healthline.com]

  • Dementia

    – may also play an important role in the onset and progression of Alzheimer’s disease.[cam.ac.uk] This early onset Alzheimer's disease can progress more rapidly than later onset AD.[medicinenet.com] Read More Mechanism behind neuron death in motor neurone disease and frontotemporal dementia discovered 20 Apr 2018 Scientists have identified the molecular mechanism that[cam.ac.uk]

  • Parkinson's Disease Type 3

    However, dementia tends to have a later onset as the disease progresses. The cause of PSP is a build-up of the protein tau, as in CBD.[parkinsonsnewstoday.com] An estimated 50 to 80 percent of those with Parkinson’s eventually experience dementia as their disease progresses.[alz.org] As with idiopathic Parkinson’s disease, progressive supranuclear palsy has a late age of onset, but the symptoms tend to progress far more rapidly once they appear.[parkinsonsnewstoday.com]

  • Young-Onset Parkinson Disease

    Generally, young-onset Parkinson’s disease has a slower disease progression and lower rate of dementia however, they tend to have increase rate of dystonia and increased rate[raredr.com] An estimated 50 to 80 percent of those with Parkinson’s eventually experience dementia as their disease progresses.[alz.org] In those diagnosed within this subset, it has been shown that there is usually a slower progression of the disease and a lower occurrence of dementia.[igeaneuro.com]

  • Parkinson's Disease

    Clinically, dementia in PD is characterized by uninsidious onset and slowly progressive cognitive decline, with a predominant dysexecutive syndrome accompanied frequently[ncbi.nlm.nih.gov] All 3 patients had early-onset l-dopa-responsive parkinsonism with dementia and frontotemporal lobar atrophy. Disease progression was relatively rapid.[ncbi.nlm.nih.gov] An estimated 50 to 80 percent of those with Parkinson’s eventually experience dementia as their disease progresses.[alz.org]

  • Hereditary Late-Onset Parkinson Disease

    Clinically the differential includes 1,3 : dementia with Lewy bodies dementia is clinically evident before, concurrently or at most within 12 months of onset of parkinsonian[radiopaedia.org] This syndrome has juvenile onset with rapid disease progression, accompanied by dementia, supranuclear gaze palsy, and pyramidal signs.[ncbi.nlm.nih.gov] […] symptoms 2 multiple system atrophy (MSA) progressive supranuclear palsy (PSP) corticobasal degeneration cerebrovascular disease metabolic diseases with parkinsonian signs[radiopaedia.org]

  • Pallidopyramidal Syndrome

    […] form of Parkinson disease similar to Pallido-pyramidal syndrome and characterized by early onset between 11 and 16 years of age, dementia, supranuclear upgaze palsy and pyramidal[cags.org.ae] […] characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain ( Gerstmann et al., 1936 ).[mendelian.co] […] the nervous system Extrapyramidal and movement disorders Mode of Inheritance Autosomal recessive Gene Map Locus Kufor-Rakeb syndrome (KRS) is a rare inherited and rapidly progressive[cags.org.ae]

  • X-linked Parkinsonism-Spasticity Syndrome

    Clinically the differential includes 1,3 : dementia with Lewy bodies dementia is clinically evident before, concurrently or at most within 12 months of onset of parkinsonian[radiopaedia.org] […] symptoms 2 multiple system atrophy (MSA) progressive supranuclear palsy (PSP) corticobasal degeneration cerebrovascular disease metabolic diseases with parkinsonian signs[radiopaedia.org] There is significant overlap between many neurodegenerative disease, and Parkinson disease is no exception.[radiopaedia.org]

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