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145 Possible Causes for Cerebellar Ataxia, Positive Romberg Sign

  • Vitamin E Deficiency

    Romberg sign) A nodding movement of the head (titubation) Decreased visual sharpness (acuity) Positive Babinski sign (upward movement of the big toe and fanning of the feet[] Subjects affected by cerebellar ataxia due to congenital isolated vitamin E deficiency (AVED) show vitamin E deficiency caused by a selective impaired gastrointestinal absorption[] Ataxia with vitamin E deficiency is an autosomal recessive cerebellar ataxia caused by mutations in the α-tocopherol transfer protein coding gene localized on chromosome 8q[]

  • Ataxia Telangiectasia

    In addition, the spinal signs involving posterior and lateral columns along the positive Romberg's sign (inability to maintain balance when the eyes are shut and feet are[] Only a mild cerebellar ataxia was present at the age of 7 years then she developed a Wilms tumor (nephroblastoma).[] These patients do, however, have scoliosis and a positive Romberg's sign.[]

  • Autosomal Dominant Sensory Ataxia

    Sensory ataxia can be distinguished from cerebellar ataxia by asking the patient to close his or her eyes.[] Romberg's sign .[] Causes of cerebellar ataxia Cerebellar ataxia can be inherited or acquired.[]

  • Cerebellar Ataxia - Neuropathy - Vestibular Areflexia Syndrome

    We propose a new name for the condition: cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS).[] All patients showed gait and limb ataxia, positive Romberg sign, cerebellar dysarthria, gaze-evoked nystagmus, absent deep tendon reflexes, and impaired vibratory sensation[] The main clinical features include bilateral vestibulopathy, cerebellar ataxia and sensory neuropathy.[]

  • Subacute Combined Degeneration of Spinal Cord

    ; and a positive Romberg test.[] ataxia ) Basal ganglia Chorea Dystonia Parkinson's disease Cortex ACA syndrome MCA syndrome PCA syndrome frontal lobe : Expressive aphasia Aboulia parietal lobe : Receptive[] ataxia in diseases classified elsewhere G32.89 Other specified degenerative disorders of nervous system in diseases classified elsewhere G35 Multiple sclerosis G36 Other[]

  • Idiopathic Bilateral Vestibulopathy

    Related Links: Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant neurodegenerative disorder characterized by cerebellar and retinal degeneration, and is caused[] They complained of oscillopsia while moving their body or head and showed positive Romberg’s signs.[] However, patients with impaired SP and OKR, usually due to cerebellar ataxia (CA), produce a near‐normal VVOR using their VOR.[]

  • Autosomal Dominant Optic Atrophy and Cataract

    Dominant Cerebellar Ataxia Type I ADCA1 - Autosomal Dominant Cerebellar Ataxia type 1 ADCAII - Autosomal Dominant Cerebellar Ataxia Type II ADCCA - Autosomal Dominant Cortical[] Romberg sign 0002403 Posterior subcapsular cataract 0007787 Red-green dyschromatopsia Red green color blindness 0000642 Resting tremor Tremor at rest 0002322 Tritanomaly[] Clinical examination at the age of 38 showed cerebellar ataxia, lower limb areflexia, pinprick and light-touch hypoesthesia, and pes cavus.[]

  • Bickerstaff Brainstem Encephalitis

    Bickerstaff brainstem encephalitis is a clinical syndrome of ophthalmoplegia, cerebellar ataxia, and central nervous system signs and is associated with the presence of anti-GQ1b[] She had positive Romberg sign and failed the right heel-knee-tibia tests.[] ataxia and areflexia after an influenza type B infection.[]

  • Argininosuccinic Aciduria

    He exhibited only moderate mental retardation, cerebellar ataxia and both abnormal hair and skin.[] Her clinical symptoms consisted of ataxia, disturbance of coordination, clumsiness, intention treMor and a positive Romberg's sign.[] She has had mild symptoms of cerebellar ataxia. Her physical growth has been below normal. Biochemical abnormalities are described.[]

  • Triple A Syndrome

    We recently discovered that the pathogenesis involved impaired nuclear import of DNA repair proteins, including DNA ligase I and the cerebellar ataxia causative protein aprataxin[] Other findings included delay of mental development, hyperreflexia , immature speech and a positive Romberg’s sign.[] ataxia, peripheral neuropathy and mild dementia) suggest that the central nervous system may be involved in the disease as well.[]

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