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Abnormalities subcortical and nonlargevessel distributed lesions ; , an increased lactate-to-pyruvate ratio in serum and CSF, and absent oligoclonal banding. Diagnosis may be aided by muscle biopsy and appropriate DNA testing. Cerebrotendinous xanthomatosis is mentioned because it may present with a progressive spinocerebellar ataxia without characteristic tendon xanthomas. It is treatable. Diagnosis is made by measuring serum cholestanol. Treatment with oral chenodeoxycholic acid may reverse or halt progressive deterioration. Hereditary Spinocerebellar Ataxias Symptoms are usually progressive, symmetric, and a family history often is present. Optic atrophy and sensory involvement may both occur but the latter is distal in distribution. Skeletal abnormalities and peripheral nerve involvement are useful distinguishing features from MS. Imaging may show atrophy, and CSF analysis is unremarkable. DNA testing may be diagnostic. Malignancy With the advent of neural axis MRI, CNS malignancy masquerading as MS is rare but should not be forgotten. Relapsing and sometimes multifocal syndromes may occur with meningiomata, gliomata, lymphoma, and metastasis, sometimes needing biopsy in ambiguous cases. Monophasic Syndromes Optic Neuritis Optic neuritis presenting with subacute unilateral visual loss may occur as a clinically isolated syndrome or as a presenting manifestation of MS. Pain with eye movement is present in 70% of patients, and a relative afferent pupillary defect confirms an optic neuropathy. A papillitis with disc swelling, perivenous sheathing, or hemorrhages may be seen. More than 90% of patients begin to show improvement by 5 weeks and attain vision of 6 12 better at one year. In children, optic neuritis is more frequently bilateral and follows viral infection. It usually has a good outcome and is rare in older age groups. Certain clinical features should prompt a search for an alternative diagnosis. Pain that restricts eye movement or wakes the patient from sleep is unusual with inflammatory optic neuritis and suggests a posterior scleritis or granulomatous condition. Papillitis.
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