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218 Possible Causes for Slowly Progressive Dysarthria

  • Unverricht-Lundborg Syndrome

    An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, dysarthria, and intention[rareomics.healx.io] progressive intellectual deterioration, dysarthria, and intention tremor.[definitions.net] 0.00 / 0 votes) Rate this definition: Unverricht-Lundborg Syndrome An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly[definitions.net]

  • Hemochromatosis

    A patient is reported with hereditary haemochromatosis and a syndrome of dementia, dysarthria, a slowly progressive gait disturbance, imbalance, muscle weakness, rigidity,[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 6

    BACKGROUND: Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder characterized by slowly progressive ataxia and dysarthria.[ncbi.nlm.nih.gov] OBJECTIVE: Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder characterized by a slowly progressive ataxia and dysarthria. Anatomically.[ncbi.nlm.nih.gov] Symptoms progress slowly, and eventually all patients have gait ataxia, upper limb incoordination, intention tremor, and dysarthria.[ataxia.uchicago.edu]

  • Dementia

    , and dysarthria.[doi.org] progressive. 13 , 14 Neurological symptoms and signs related to SVD include cognitive deterioration, gait disturbance (imbalance, fall, short-stepped gait), urinary dysfunction[doi.org] The onset of SVD is insidious in over half of patients and the course is usually continuous and slowly progressive. 13, 14 Neurological symptoms and signs related to SVD include[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 14

    CLINICAL CHARACTERISTICS: Spinocerebellar ataxia type 14 (SCA14) is characterized by slowly progressive cerebellar ataxia, dysarthria, and nystagmus.[ncbi.nlm.nih.gov] The condition progresses slowly.[checkorphan.org] , nystagmus, partial complex and generalized motor seizures, tremor, spasticity, Mexican families SCA11 (autosomal dominant type 11) 15q14-q21.3 Slowly progressive gait and[bcm.edu]

  • Primary Lateral Sclerosis

    The spasticity slowly progressed, and she died of aspiration pneumonia 3.5 years after the onset of dysarthria.[ncbi.nlm.nih.gov] We report an autopsy case of progressive supranuclear palsy (PSP) that clinically showed only slowly progressive and symmetric upper motor neuron syndrome over a disease course[ncbi.nlm.nih.gov] Slowly progressive isolated dysarthria: longitudinal course, speech features, and neuropsychological deficits.[ncbi.nlm.nih.gov]

  • Ischemic Peripheral Neuropathy

    By contrast, chronic progressive NB is characterized by intractable slowly progressive dementia, ataxia and dysarthria, with persistent elevation of cerebrospinal fluid (CSF[ncbi.nlm.nih.gov]

  • Systemic Vasculitis

    By contrast, chronic progressive NB is characterized by intractable slowly progressive dementia, ataxia and dysarthria, with persistent elevation of cerebrospinal fluid (CSF[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 20

    CLINICAL CHARACTERISTICS: Spinocerebellar ataxia type 20 (SCA20) is characterized by a slowly progressive ataxia and dysarthria.[ncbi.nlm.nih.gov] Spinocerebellar ataxia type 20 (SCA20) is characterized by a slowly progressive ataxia and dysarthria.[ncbi.nlm.nih.gov] The age at onset ranges from teenage years to late adulthood, and the disorder is slowly progressive.[diseaseinfosearch.org]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Autosomal dominant cerebellar ataxia (ADCA) describes a clinically and genetically heterogeneous group of neurodegenerative diseases characterized by a slowly progressive[monarchinitiative.org] Systemic Features: Symptoms have their onset in late childhood and are slowly progressive. Walking and balancing are difficult.[disorders.eyes.arizona.edu] Slow progression -- 11p13 Mutation in SPTBN2 gene Spinocerebellar ataxia (SCA6) OMIM #183086 Slowly progressive, pure cerebellar ataxia with dysarthria, nystagmus Occasional[emedicine.medscape.com]

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