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47 Possible Causes for Cerebellar Gait Ataxia, Poor Coordination of the Lower Extremity

  • Acute Cerebellar Ataxia

    Truncal ataxia with deterioration of gait Slurred speech and nystagmus Afebrile Possible causes of acute cerebellar ataxia include varicella infection, as well as infection[] Acute cerebellar ataxia is a clinical syndrome with sudden onset of uncoordinated gait and normal mental status in young children.[] AIM: Acute cerebellar ataxia (ACA, sudden onset of truncal ataxia and gait disturbances) usually follows a benign illness (25% varicella).[]

  • Alcoholic Cerebellar Degeneration

    Definition / general Atrophy of the cerebellar vermis seen in the setting of chronic alcoholism Essential features Characterized clinically by ataxia and gait disturbances[] […] affects stance, eye movements, and gait, sometimes with trunkal ataxia and titubation.[] Cerebellar ataxia differs from gait problems due to abnormalities in other parts of the nervous system, such as the abnormal gait seen in Parkinson’s disease, normal pressure[]

  • Peripheral Neuropathy

    All patients have gait ataxia and the majority have lower limb ataxia.[] GA is usually of insidious onset; however, it can also be rapidly progressive mimicking paraneoplastic cerebellar degeneration. Gaze-evoked nystagmus is common.[]

  • Spinocerebellar Ataxia Type 13

    SCA8 SCA-8 is a slowly progressive ataxia resulting in poor coordination of limbs, especially lower extremities, and poor coordination of gait and speech.[] The patients-seven women and a 4-year-old boy-exhibited slowly progressive childhood-onset cerebellar gait ataxia associated with cerebellar dysarthria, moderate mental retardation[] Poor Co-ordination- The function of upper and lower extremity muscles are affected, because of lack of normal coordination.[]

  • Hereditary Cerebellar Degeneration

    cerebellar ataxia can improve ataxia, gait ability, and activity of daily living.[] Key Concepts Clinical syndromes associated with cerebellar dysfunction may be divided into syndromes that predominantly affect the midline cerebellar structures (gait and[] Other neurodegenerative disorders, such as Parkinson's disease and multiple sclerosis, may present cerebellar and/or gait ataxia as one of the clinical signs.[]

  • Ataxia Telangiectasia

    Abstract Ataxia Telangiectasia (AT) is named after the two key clinical features that characterize its classical phenotype, namely a progressive cerebellar gait disorder ([] Symptoms include: Decreased coordination of movements (ataxia) in late childhood that can include ataxic gait (cerebellar ataxia ), jerky gait, unsteadiness Decreasing mental[] ataxia) and vascular anomalies (telangiectasias) visible in the conjunctivae and skin.[]

  • 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.[] Midline cerebellar degeneration (also referred to as alcoholic cerebellar degeneration) is a component of WKS, but may also occur alone.[]

  • Cerebellar Neoplasm

    Plasma exchange Ataxia with antibodies to CARP 8 10 Epidemiology: 1 patient; 77 year old female Clinical: Pure cerebellar syndrome Onset: 3 years after neoplasm Ataxia: Limb[] Effects of axial weight loading on gait for subjects with cerebellar ataxia: preliminary findings. Neurology Report 27, 1, 2003, 15-21 Giordano, I., et al. (2017).[] : Ataxia Most common feature of Ri syndrome (50%) Truncal ataxia & Gait disorder Dysarthria: Rare Nystagmus: 33% Other associated disorders in some patients Myelopathy (18%[]

  • Autosomal Recessive Spinocerebellar Ataxia 18

    -18 is a neurologic disorder characterized by delayed psychomotor development, severely impaired gait due to cerebellar ataxia, ocular movement abnormalities, and intellectual[] SCA8 SCA-8 is a slowly progressive ataxia resulting in poor coordination of limbs, especially lower extremities, and poor coordination of gait and speech.[] Affiliated tissues include skeletal muscle, and related phenotypes are muscle weakness and gait ataxia Disease Ontology : 12 An autosomal dominant cerebellar ataxia that is[]

  • Friedreich Ataxia

    Rehabilitation Of Limb And Gait Ataxia In Hereditary Cerebellar Ataxias: A Pilot Open-Labeled Study ,” published in the journal Neurological Sciences.[] […] in patients affected by hereditary cerebellar ataxias.[] There are a wide variety of potential clinical manifestations 11 : neurological cerebellar and spinocerebellar tract involvement: four-limb ataxia, gait ataxia, cerebellar[]

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