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1,290 Possible Causes for Dementia, Huntington's Disease, Motor Symptoms

  • Parkinson's Disease

    Olfactory deficit is considered the most common NMS in PD preceding the motor symptoms for years.[ncbi.nlm.nih.gov] Assessment of Caregiver Burden in Huntington's Disease. Yu M, Tan K, Koloms K, Bega D. J Huntingtons Dis. 2019;8(1):111-114. doi: 10.3233/JHD-180326.[parkinsons.northwestern.edu] […] disease dementia (PDD), together known as the Lewy body dementias.[ncbi.nlm.nih.gov]

  • Huntington's Disease

    In addition, multiple regressions were performed to investigate the impact of family history on the age at onset of depression and motor symptoms.[ncbi.nlm.nih.gov] […] movements, behavioral and psychiatric disturbances and dementia HD Huntington's chorea Huntington’s disease Huntington Chorea Huntington's disease HUNTINGTON DISEASE; HD[wikidata.org] Dementias: Advances in Neurology. 38 Vol. New York, NY: Raven; 1983. Meiser B, Dunn S.[web.archive.org]

  • Progressive Supranuclear Palsy

    All these non-motor symptoms in PSP mimicked those of multiple system atrophy.[ncbi.nlm.nih.gov] More common differential diagnosis may include [10] : Alzheimer’s Disease Apraxia and Related Syndromes Multisystem Atrophy Huntington’s Disease Dizziness, Vertigo and Imbalance[physio-pedia.com] However, the subcortical dementias can be clearly distinguished clinically from cortical dementias, other than frontal dementias.[doi.org]

  • Parkinson-Dementia Syndrome

    Turning on the subthalamic nucleus electrodes improved motor symptoms but left cognitive performance almost unchanged.[ncbi.nlm.nih.gov] Huntington’s Disease Related Dementia Huntington’s disease (HD) is a genetic disease that is connected with, or may contribute to dementia.[dementiacarecentral.com] RESULTS: Turning on the subthalamic nucleus electrodes improved motor symptoms but left cognitive performance almost unchanged.[f1000.com]

  • Secondary Parkinsonism

    BACKGROUND: Non-Motor Symptoms (NMS) are frequent in patients with Idiopathic Parkinson's Disease (IPD).[clinicaltrials.gov] disease ( G10 ) • Shy-Drager syndrome ( G90.3 ) • syphilitic Parkinsonism ( A52.19 )[coding-pro.com] (eg, Alzheimer disease, chromosome 17–linked frontotemporal dementias, diffuse Lewy body dementia) Parkinsonism often preceded by dementia most typically with Prominent memory[msdmanuals.com]

  • Juvenile Huntington Disease

    This report raises the possibility that use of dopaminergic agonists in patients with a family history of Huntington disease may lead to clinical exacerbation of motor symptoms[ncbi.nlm.nih.gov] Abstract Of 195 cases of juvenile Huntington disease gathered from case descriptions, the sex, age at onset, duration of disease, clinical type, sex of the affected parent[ncbi.nlm.nih.gov] Like the adult form of the disorder, JHD is a hereditary neurodegenerative disease characterized by dementia and behavioral changes, caused by an expanded CAG repeat within[ncbi.nlm.nih.gov]

  • Parkinson's Disease Type 3

    The Parkinson’s community acknowledges that there are many important non-motor symptoms as well as motor symptoms.[parkinson.org] Pantothenate kinase-associated neurodegeneration, juvenile Huntington disease (see these terms) and central basal ganglia lesions.[orpha.net] […] or Lewy body dementia.[alz.org]

  • Hallervorden-Spatz Syndrome

    Patients with HSS/NBIA have a combination of motor symptoms in the form of dystonia, parkinsonism, choreoathetosis, corticospinal tract involvement, optic atrophy, pigmentary[ncbi.nlm.nih.gov] In this respect, HSS may serve as a model for complex neurodegenerative diseases, such as Parkinson disease, Alzheimer disease, Huntington disease and human immunodeficiency[ncbi.nlm.nih.gov] Serial assessments of a 29-year-old woman showed progressive dementia.[ncbi.nlm.nih.gov]

  • Huntington Disease-Like 3

    […] with motor symptoms.[e-jmd.org] disease and mimicking disorders called Huntington's disease -like (HDL) phenotypes.[journals.lww.com] Like Huntington's disease (HD), it is an adult onset, progressive, neurodegenerative autosomal dominant disorder clinically characterized by abnormal movements, dementia,[jhu.pure.elsevier.com]

  • Postencephalitic Parkinson Disease

    […] disease, but they also experience non-motor symptoms (NMS) that are often present before diagnosis or that inevitably emerge with disease progression.[books.google.de] Many neurological diseases, such as Huntington's disease, Friedreich's ataxia, and multiple sclerosis, are associated with progressive memory deficits.[books.google.com] Seite 177 - ... by vomiting and severe diarrhea Delusions: beliefs that are firmly held despite proof that they are false Dementia: a progressive decline in mental functions[books.google.de]

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