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24 Possible Causes for Cerebellar Gait Ataxia, Nocturnal Leg Cramp, Progressive Polyneuropathy

  • Chronic Alcoholism

    The cause of the alcoholic gait is brain damage called alcoholic cerebellar ataxia.[promises.com] Both balance and gait are compromised. Can an Alcoholic Recover from Cerebellar Ataxia?[promises.com] However, long-term alcoholics frequently develop cerebellar ataxia. It’s called cerebellar ataxia, because it affects a part of the brain called the cerebellum.[promises.com]

  • Pernicious Anemia

    It causes ataxia of stance and gait with relative sparing of the arms. It has an insidious onset and a subacute or chronic course.[neuropathology-web.org] Midline cerebellar degeneration (also referred to as alcoholic cerebellar degeneration) is a component of WKS, but may also occur alone.[neuropathology-web.org]

  • Alcoholic Neuropathy

    […] of alcoholic polyneuropathy.[en.wikipedia.org] Limb or gait ataxia was prominent in 3 patients. Ataxia was of sensory type, and 1 patient additionally showed features of cerebellar ataxia.[jamanetwork.com] Results: Symmetric sensory-dominant polyneuropathy predominantly involving the lower limbs was the major clinical pattern.[n.neurology.org]

  • Peripheral Neuropathy

    Most types of polyneuropathy progress fairly slowly, over months or years, but rapidly progressive polyneuropathy also occurs.[en.wikipedia.org] All patients have gait ataxia and the majority have lower limb ataxia.[doi.org] The primary manifestations of polyneuropathy are slowly progressive numbness and paresthesias, with burning sensations in the feet usually in a symmetrical pattern.[ncbi.nlm.nih.gov]

  • Spastic Paraplegia

    Complex HSP involves additional neurologic symptoms and signs like ataxia, extra pyramidal signs, polyneuropathy, and cognitive decline.[ojrd.biomedcentral.com] Main inclusion criteria for HA were cerebellar gait and/or limb ataxia, and for HSP, spasticity in the lower limbs, brisk reflexes and positive Babinski sign [ 11, 12 ].[journals.plos.org] gait.[nature.com]

  • Autosomal Recessive Spastic Paraplegia Type 48

    Polyneuropathy Type) X-Linked Adrenoleukodystrophy Causes List for Paralysis List of possible causes of Paralysis or similar symptoms may include: 8 ATR-X syndrome (Hemiplegia[familydiagnosis.com] Abstract Background: Hereditary cerebellar ataxias (HCA) and hereditary spastic paraplegias (HSP) are two groups of neurodegenerative disorders that usually present with progressive[karger.com] She first noticed gait disturbance and spasticity in the lower extremities together with nocturnal leg cramps and pain attacks in the upper limbs at age of 28 years.[omicsonline.org]

  • Muscular Fasciculation

    多発性ニューロパチ(シ)ー、多発性神経障害 positron emission tomography (PET) 陽電子断層撮影法 progressive bulbar palsy進行性球[延髄]麻痺 progressive muscular dystorophy進行性筋ジストロフィ progressive paralysis進行性麻痺 psychomotor[tokyo-med.ac.jp] There are two major forms of cerebellar ataxia. Disturbances of posture or gait result from lesions to the vestibulocerebellum.[nba.uth.tmc.edu] Nocturnal leg cramps are involuntary muscle contractions that occur typically in the leg muscles at night or during rest.[spine.org]

  • Autosomal Recessive Spastic Paraplegia Type 18

    CMT2X patients manifest a slowly progressive, peripheral neuropathy affecting the lower limbs and resulting in gait difficulties and distal sensory impairment.[genecards.org] Other early signs of cerebellar ataxia include dysarthria and nystagmus. The spasticity is progressive and eventually dominates the clinical picture.[orpha.net] She first noticed gait disturbance and spasticity in the lower extremities together with nocturnal leg cramps and pain attacks in the upper limbs at age of 28 years.[omicsonline.org]

  • Autosomal Recessive Spastic Paraplegia Type 14

    Finally, disease progression seemed slow as all patients were able to walk after disease durations up to 15 years.[academic.oup.com] She first noticed gait disturbance and spasticity in the lower extremities together with nocturnal leg cramps and pain attacks in the upper limbs at age of 28 years.[omicsonline.org] Abstract Background: Hereditary cerebellar ataxias (HCA) and hereditary spastic paraplegias (HSP) are two groups of neurodegenerative disorders that usually present with progressive[karger.com]

  • Autosomal Recessive Spastic Paraplegia Type 39

    CMT2X patients manifest a slowly progressive, peripheral neuropathy affecting the lower limbs and resulting in gait difficulties and distal sensory impairment.[genecards.org] The overall picture was spastic gait with variable associated distal wasting, sensory neuropathy and cerebellar ataxia ( Table 2 ).[academic.oup.com] She first noticed gait disturbance and spasticity in the lower extremities together with nocturnal leg cramps and pain attacks in the upper limbs at age of 28 years.[omicsonline.org]

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