Create issue ticket

36 Possible Causes for Dementia, Involuntary Tongue Protrusion, Rapid Progression

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Disease progression was rapid, and the majority of patients died from respiratory failure within 1–5 years after onset of disease.[link.springer.com] […] choreic movements, mild alteration in personality, grimacing, protrusion of the tongue and ataxia with choreoathetoid movements -Later stages include mental deterioration[quizlet.com] Access comprehensive discussions of Alzheimer and commonly occurring non-Alzheimer dementias (such as Lewy bodies disease and frontotemporal dementia) and traumatic brain[books.google.com]

  • Rett Syndrome

    We herein report the surgical result of treating severe rapid progressive thoracic scoliosis in a 16-year-old girl with Rett syndrome.[ncbi.nlm.nih.gov] […] movements of the upper limbs and tongue protrusion.[ncbi.nlm.nih.gov] Rett syndrome Rett syndrome w dementia Rett syndrome w dementia w behavioral disturbance Rett's disorder Retts syndrome Retts syndrome with dementia Clinical Information[icd10data.com]

  • Huntington Disease-Like 2

    Mean survival time is 1 to 10 years, and rapid progression is suspicious of this cause.[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] We report on a South African family that presented with progressive dementia and a movement disorder affecting numerous family members.[ncbi.nlm.nih.gov]

  • Huntington Disease-Like 3

    progression Trinucleotide cytosine-adenine-guanine (CAG) repeat expansion Length of repeat is inversely associated with, but is not an accurate predictor of, age of onset[unboundmedicine.com] 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]

  • Huntington Disease-Like 1

    Mean survival time is 1 to 10 years, and rapid progression is suspicious of this cause.[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] Gerstmann-Straussler disease (sequence analysis of PRNP gene) Insomnia, fatal familial (sequence analysis of PRNP gene) Hereditary chorea (WES based NGS panel for 14 genes) Frontotemporal dementia[cgcgenetics.com]

  • Senile Chorea

    It has a more rapid progression, accompanied by mental disorders (depression, tendency to suicide, hallucinations), intellectual decline until dementia.[medicalformat.com] 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

    Progressive supranuclear palsy. 7 Myoclonus?[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]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Mean survival time is 1 to 10 years, and rapid progression is suspicious of this cause.[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]

  • McLeod Neuroacanthocytosis Syndrome

    progression) or atypical disease (later onset with slow progression).[scienceopen.com] 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]

  • Spinocerebellar Ataxia Type 6

    However several new clinical features were found in some patients: dramatic anticipation, rapid disease progression, severe ataxia associated with action tremor or action[ncbi.nlm.nih.gov] They consisted of jaw-opening dystonia with almost rhythmic tongue protrusion, consistent with the dystonic tremor of the tongue (see Video 2, part IIIb).[movementdisorders.org] During this period, eye movement becomes slower down and some patient also has dementia in the latter stage of life.[healthsaline.com]

Similar symptoms