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229 Possible Causes for Behavior Problem, Cerebellar Gait Ataxia, Spastic Gait

  • Primary Progressive Multiple Sclerosis

    A 28-year-old woman developed progressive spastic gait and dysarthria.[] […] and visual defects, muscular weakness, absent abdominal reflexes, hyperactive tendon reflexes, cerebellar ataxia, retrobulbar neuritis, loss of proprioceptive sense, spastic[] Also known as progressive myelopathy, these symptoms may include: Spastic paraparesis : An increasingly spastic gait in which your legs will begin to stiffen, causing a visible[]

  • Huntington's Disease

    At age 48, rigidity and spastic gait were observed. One year later, choreoathetoid involuntary movements became apparent.[] […] dysfunction masquerading dominant spinocerebellar ataxias (SCA), were occasionally reported.[] Behavioral Problems in Huntington’s Disease. A helpful guide for coping with and caring for individuals experiencing the behavioral symptoms of HD. Paulsen, J.[]

  • Subacute Combined Degeneration of Spinal Cord

    Numbness of the limbs and trunk is an early symptom; weakness, clumsiness and spasticity, abnormal reflexes, gait ataxia develop later.[] It causes ataxia of stance and gait with relative sparing of the arms. It has an insidious onset and a subacute or chronic course.[] […] paresis Gait abnormalities (spinal ataxia, positive Romberg's test ) Neuropsychiatric disease (e.g., dementia, depression, paranoia ) Worsening vision Autonomic dysfunction[]

  • Cerebral Palsy

    BACKGROUND: Previous researchers reported that popliteal angle did not correlate well with knee angle during gait in individuals with spastic cerebral palsy (CP).[] GA usually presents with pure cerebellar ataxia primarily affecting gait and lower limbs.[] Some behavioral problems are extreme irritability, feeding difficulties, persistent gagging or choking when fed after 6 months of age especially if the tongue pushes the food[]

  • Pallidopyramidal Syndrome

    […] disorder characterized predominantly by spasticity and muscle weakness of the lower limbs, resulting in gait difficulties and loss of ambulation in some patients.[] […] disorder (RBD), hallucinations and thinking problems which can lead to dementia.[] .  Cerebellar dysfunction :  A. Features  1. Gait ataxia  2. Ataxic dysarthria  3. Limb ataxia  4.[]

  • Wernicke Encephalopathy

    Other neurologic deficits include paresis, spasticity, gait disturbance, speech disorders, coma, dementia, Parkinsonism, chorea, tremors, dystonia, myoclonia, and orthostatic[] ., nystagmus, ophthalmoplegia) and cerebellar dysfunction (e.g., gait disturbance, ataxia) define this condition.[] However, even if the person stops drinking and replenishes thiamine, symptoms of the disease (e.g., problem behaviors, agitation, lack of coordination, learning deficits)[]

  • Upper Motor Neuron Disease

    Although muscle weakness is present, the main deficits are due to spasticity in dexterity and gait.[] There are two major forms of cerebellar ataxia. Disturbances of posture or gait result from lesions to the vestibulocerebellum .[] This includes difficulties with memory, planning, language, behavior, and spatial relationships.[]

  • Autosomal Dominant Spastic Paraplegia Type 8

    SPG4 is characterized by insidiously progressive bilateral lower-limb gait spasticity.[] None had cerebellar gait ataxia but a mild cerebellar syndrome in the upper limbs was diagnosed in four patients.[] Behavior problems are common having features of ADHD, autism, and aggression. Foot deformities have been noted.[]

  • Autosomal Recessive Spastic Paraplegia Type 26

    Background: Hereditary spastic paraplegias (HSP) are degenerative diseases of upper motor neurons characterized by a progressive spastic gait disorder which are phenotypically[] Abstract Background: Hereditary cerebellar ataxias (HCA) and hereditary spastic paraplegias (HSP) are two groups of neurodegenerative disorders that usually present with progressive[] problems.[]

  • Pernicious Anemia

    […] and abnormal gait PNS Manifestations Neuropathy motor-sensory polyneuropathy (parasthesias, numbness and weakness) mononeuropathy (optic or olfactory) autonomic neuropathy[] It causes ataxia of stance and gait with relative sparing of the arms. It has an insidious onset and a subacute or chronic course.[] Less frequently, patients with PA may present only with neurological symptoms, such as paresthesia, unsteady gait, clumsiness, and in some cases, spasticity.[]

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