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4,855 Possible Causes for Dementia, Involuntary Tongue Protrusion, Trinucleotide Repeat Expansion in the JPH3 Gene

  • Huntington Disease-Like 2

    Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.[ncbi.nlm.nih.gov] 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

    Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain. 2003 Jul;126(Pt 7):1599-603. Epub 2003 May 6.[ghr.nlm.nih.gov] 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]

  • Huntington Disease-Like 3

    Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain. 2003 Jul;126(Pt 7):1599-603. Epub 2003 May 6.[ghr.nlm.nih.gov] 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]

  • Late-onset Depression

    Symptoms Tardive dyskinesia causes repetitive, involuntary, and purposeless movements and tics often in the face such as: Worm-like tongue movements Lip smacking Chewing or[verywellmind.com] (AD) or a vascular dementia, as these are by far the most common causes of dementia.[ncbi.nlm.nih.gov] Dementia types were as follows: 73% Alzheimer disease, 24% vascular and mixed dementia, and 3% Parkinson dementia.[ncbi.nlm.nih.gov]

    Missing: Trinucleotide Repeat Expansion in the JPH3 Gene
  • Huntington's Disease

    Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.[ncbi.nlm.nih.gov] Dementias: Advances in Neurology . 38 Vol. New York, NY: Raven; 1983. Meiser B, Dunn S.[web.archive.org] Stevanin G et al. (2003) Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain 126 : 1599–1603 15.[dx.doi.org]

    Missing: Involuntary Tongue Protrusion
  • Orofacial Dyskinesia

    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] […] pouting of the lips, and tongue protrusions.[en.wikipedia.org]

    Missing: Trinucleotide Repeat Expansion in the JPH3 Gene
  • Rett Syndrome

    […] 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] . & Kerbeshian, J. (1989) Pervasive disintegrative disorders: Are Rett syndrome and Heller dementia infantilis subtypes?[doi.org]

    Missing: Trinucleotide Repeat Expansion in the JPH3 Gene
  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.[ncbi.nlm.nih.gov] However, clinical characteristics such as dystonia with prominent orofacial involvement with tongue protrusion, involuntary tongue- and lip-biting, head thrusts, and rubber[movementdisorders.org] It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.[orpha.net]

  • Jankovic Rivera Syndrome

    Huntington’s disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain 2003;126(Pt 7):1599–1603. 145.[e-jmd.org] Symptoms - Jankovic Rivera syndrome * Progressive distal muscle weakness * Progressive distal muscle wasting * Myoclonic jerks * Dementia * Abnormal walk * Speech defect Causes[checkorphan.org] Gibbs, Syndromes of amyotrophic lateral sclerosis and dementia: Relation to transmissible Creutzfeldt‐Jakob disease, Annals of Neurology, 14, 1, (17-26), (2004).[doi.org]

  • McLeod Neuroacanthocytosis Syndrome

    Huntington’s disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain 2003;126(Pt 7):1599–1603. 145.[e-jmd.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] . • A variety of other neurologic symptoms may accompany neuroacanthocytosis, including seizures, motor neuron disease, and dementia.[medlink.com]

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