Spinocerebellar ataxia 2
Overview
Spinocerebellar ataxia 2: A disorder involving degeneration of the brain and spinal cord and causing progressive coordination difficulty and other symptoms. Symptom generally become more severe earlier than in spinocerebellar ataxia 1.
Symptoms
Spinocerebellar degeneration Abnormal eye movements Absent eye scanning Slow eye tracking Progressive mental deterioration
Causes
Cerebellar abscess. Cerebellar abscess commonly causes limb ataxia on the same side as the lesion as well as gait and truncal ataxia. Typically, the initial symptom is a headache localized behind the ear or in the occipital region, followed by oculomotor palsy, fever, vomiting, an altered LOC, and coma. Cerebellar hemorrhage. With cerebellar hemorrhage, a life-threatening disorder, ataxia is usually acute but transient. Unilateral or bilateral ataxia affects the trunk, gait, or limbs. The patient initially experiences repeated vomiting, occipital headache, vertigo, oculomotor palsy, dysphagia, and dysarthria. Later signs, such as a decreased LOC or coma, signal impending herniation. Creutzfeldt-Jakob disease. Creutz-feldt-Jakob disease is a rapidly progressive dementia accompanied by neurologic signs and symptoms, such as myoclonic jerking, ataxia, aphasia, visual disturbances, and paralysis. It generally affects adults ages 40 to 65. Diabetic neuropathy. Peripheral nerve damage due to diabetes mellitus may cause sensory ataxia, extremity pain, slight leg weakness, skin changes, and bowel and bladder dysfunction. Diphtheria. Within 4 to 8 weeks of the onset of ymptoms, a life-threatening neuropathy can produce sensory ataxia. Diphtheria can be accompanied by fever, paresthesia, and paralysis of the limbs and, sometimes, the respiratory muscles. Encephalomyelitis. Encephalomyelitis a complication of measles, smallpox, chickenpox, or rubella or of rabies or smallpox vaccination that may damage cerebrospinal white matter. Rarely, it’s accompanied by cerebellar ataxia. Other signs and symptoms include headache, fever, vomiting, an altered LOC, paralysis, seizures, oculomotor palsy, and pupillary changes.
Prognosis
The 'prognosis' of Spinocerebellar ataxia 2 usually refers to the likely outcome of Spinocerebellar ataxia 2. The prognosis of Spinocerebellar ataxia 2 may include the duration of Spinocerebellar ataxia 2, chances of complications of Spinocerebellar ataxia 2, probable outcomes, prospects for recovery, recovery period for Spinocerebellar ataxia 2, survival rates, death rates, and other outcome possibilities in the overall prognosis of Spinocerebellar ataxia 2. Naturally, such forecast issues are by their nature unpredictable.