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1,237 Possible Causes for Gait Ataxia

  • Vitamin B12 Deficiency

    He developed aggression, urinary incontinence, gait ataxia, and memory disturbances and was admitted.[doi.org] It can be a cause of unsteady gait (ataxia), sometimes accompanied by anemia (macrocytic), and loss of position sense.[dizziness-and-balance.com] Paresthesia - numbness, tingling and pain Confusion / disorientation Weakness of legs, arms, trunk Impaired vibration - position sense Abnormal reflexes Unsteady or abnormal gait[b12deficiency.info]

  • Amyotrophic Lateral Sclerosis

    Clinical examination, 20 years after the onset of the patient's symptoms, revealed that the boxer had tremor, gait ataxia and pyramidal tract dysfunction, but possessed normal[doi.org]

  • Niemann-Pick Disease Type C

    It is characterized clinically by a variety of progressive, disabling neurological symptoms including clumsiness, limb and gait ataxia, dysarthria, dysphagia and cognitive[ncbi.nlm.nih.gov] Neurological examination at Mayo Clinic revealed oromandibular dystonia, an ataxic and hypokinetic dysarthria, mild hyperreflexia, and gait ataxia.[jnnp.bmj.com] , clumsiness, problems in walking (ataxia) Difficulty in posturing of limbs (dystonia) Slurred, irregular speech (dysarthria) Learning difficulties and progressive intellectual[npuk.org]

  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

    At the age of 6 years, the boy had no acute encephalopathy or pyramidal signs, but did exhibit mild clumsiness and subtle gait ataxia (only evident on tandem walking).[hkmj.org] The characteristic neurological picture may include spastic gait, pyramidal tract signs, seizures and ataxia.[journals.lww.com] Intermittent ataxia: unstable gait ,dysmetria. periodic ammonia Intellectual impairment: Episodic hyperammonemia may produce subtle intellectual deficits even in clinically[slideshare.net]

  • Hyperammonemia Type 3

    Intermittent ataxia: unstable gait ,dysmetria. periodic ammonia Intellectual impairment: Episodic hyperammonemia may produce subtle intellectual deficits even in clinically[slideshare.net]

  • Arnold Chiari Malformation

    General Information Chiari malformation is a general term used to describe a condition when the bottom part of the cerebellum (the “tonsils”) dip down into the upper spinal canal. (Figure legend: MRI image of the base of the brain showing the cerebellar tonsil (outlined by the six arrowheads) below the base of the[…][web.archive.org]

  • Ataxia

    Here, we report two new cases of anti-Ca-associated autoimmune cerebellar ataxia. Patient 1 presented with dizziness and acute yet mild limb and gait ataxia.[ncbi.nlm.nih.gov] A 3-year-old male presented with apparent progressive gait ataxia and non-specific leg pain. Initial imaging was unremarkable.[ncbi.nlm.nih.gov] Here, we report a Han Chinese family with SCA18; the family members presented with a slowly progressing gait ataxia, pyramidal tract signs, and peripheral neuropathy.[ncbi.nlm.nih.gov]

  • Hereditary ATTR Amyloidosis

    Hereditary ATTR amyloidosis is a progressively fatal genetic disease caused by an accumulation of transthyretin in the liver and several other organs. The diagnosis is made by biopsy and supportive imaging studies. Liver transplantation is currently the mainstay of therapy. Novel treatment strategies are being[…][symptoma.com]

  • Cerebellar Ataxia

    RESULTS: We described four patients with cerebellar ataxia, predominantly gait ataxia, due to statins use.[ncbi.nlm.nih.gov] Here, we report two new cases of anti-Ca-associated autoimmune cerebellar ataxia. Patient 1 presented with dizziness and acute yet mild limb and gait ataxia.[ncbi.nlm.nih.gov] ) gait item as the most valid and responsive measures of gait in cerebellar ataxia.[ncbi.nlm.nih.gov]

  • Homocystinuria

    Patients who become symptomatic beyond infancy may present with ataxia, dementia or psychosis.[orpha.net] Patients with cblD present with severe learning difficulties, behavioral problems and movement and gait abnormalities and patients with cblF and cblJ present with feeding[orpha.net]

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