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13 Possible Causes for Atrophy of the Caudate, Dementia, Involuntary Tongue Protrusion

  • Huntington Disease-Like 3

    […] and bilateral caudate atrophy.[orpha.net] However, clinical characteristics such as dystonia with prominent orofacial involvement with tongue protrusion, involuntary tongue- and lip-biting, head thrusts, and rubber[movementdisorders.org] 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]

  • Orofacial Dyskinesia

    MRI was negative for white matter changes and caudate atrophy.[neurology.org] Keywords Lower Face Botulinum Toxin Injection Tongue Protrusion Dystonic Movement Tardive Dystonia These keywords were added by machine and not by the authors.[link.springer.com] Patients with Alzheimer's disease, vascular dementia or mixed dementia who had indications for neuroleptic therapy were enrolled in a one-year, open-label study.[aafp.org]

  • Huntington Disease-Like 2

    On imaging, it is classically characterized by atrophy of the caudate nucleus with concomitant enlargement of the frontal horns of the lateral ventricles.[radiopaedia.org] However, clinical characteristics such as dystonia with prominent orofacial involvement with tongue protrusion, involuntary tongue- and lip-biting, head thrusts, and rubber[movementdisorders.org] Abstract Huntington disease-like 2 (HDL2) is an autosomal dominant disorder characterized by adult-onset, progressive motor abnormalities, psychiatric disturbances, and dementia[ncbi.nlm.nih.gov]

  • Huntington Disease-Like 1

    On imaging, it is classically characterized by atrophy of the caudate nucleus with concomitant enlargement of the frontal horns of the lateral ventricles.[radiopaedia.org] However, clinical characteristics such as dystonia with prominent orofacial involvement with tongue protrusion, involuntary tongue- and lip-biting, head thrusts, and rubber[movementdisorders.org] […] aggressiveness, manias, anxiety and/or depression in conjunction with rapidly progressive cognitive decline (presenting with dysarthria, apraxia, aphasia, and eventually leading to dementia[orpha.net]

  • McLeod Neuroacanthocytosis Syndrome

    We emphasize the prominent neurological picture characterized by a choreic syndrome with atrophy of the caudate nucleus on MRI, psychiatric disturbances, peripheral nerve[ncbi.nlm.nih.gov] These symptoms may be referred to as orofacial and lingual dyskinesia and include protrusion of the tongue, grimacing, and abnormal jaw movements.[rarediseases.org] . • A variety of other neurologic symptoms may accompany neuroacanthocytosis, including seizures, motor neuron disease, and dementia.[medlink.com]

  • Senile Chorea

    […] or atrophy of the caudate head Treatment : Dopamine Blockers (Haloperidol) 1.2 Sydenham's Chorea Seen mostly in teenage girls, a third of whom will have rheumatic heart disease[academic.sun.ac.za] It usually affects orofacial and lingual musculature (“buccolinguomasticatory syndrome”) with chewing; bruxism; protrusion, curling, or twisting of the tongue; lip smacking[mdedge.com] Senile chorea (SC) is characterized by the presence of late onset, generalized chorea with no family history and no dementia.[ncbi.nlm.nih.gov]

  • Extrapyramidal Disorder

    Is unclear ,in some it associated with atrophy (cell loss) of caudate and putamen.[slideplayer.com] Involuntary jaw opening. Lateral movements of the jaw. Protrusion of the tongue. Present during the day. Disappears during deep sleep.[pocketdentistry.com] Assessment of associated features provided no evidence that cerebral vascular disease might be the cause of the combination of dementia with extrapyramidal features.[karger.com]

  • Chorea Acanthocytosis Syndrome

    The caudate nucleus head atrophy demonstrated a dorsal to ventral pattern (marked by yellow), while the putamen presented a caudate to rostral mode (marked by black).[journal.frontiersin.org] These symptoms may be referred to as orofacial and lingual dyskinesia and include protrusion of the tongue, grimacing, and abnormal jaw movements.[rarediseases.org] Fragile X Tremor Ataxia Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias; Metabolic Disorders; Friedreich Ataxia; ALS; Dementia[books.google.com]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Imaging features are similar to ChAc, that is, atrophy of the caudate nucleus and putamen.[movementdisorders.org] It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.[orpha.net] Dementia HRQL Instruments Not Optimized Although a number of HRQL instruments for dementia are available, their use to date may not be optimized, researchers have concluded[practicalneurology.com]

  • Familial Dyskinesia and Facial Myokymia

    Imaging features are similar to ChAc, that is, atrophy of the caudate nucleus and putamen.[movementdisorders.org] No pyramidal, dementia or extrapyramidal findings occur. Patients are non-ambulatory within 20 years after onset.[neuroweb.us] Dear Readers, We invite you to read the following article recommendations, prepared for you by our Scientific Panels: Dementia and cognitive disorders, Higher cortical functions[eanpages.org]

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