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Patients typically have subacute onset of asymmetric, non\u2013length\u2010dependent sensory impairment and early ataxia. The etiologies of acquired sensory neuronopathies are rather limited. Early identification is imperative, as they may herald an underlying malignancy or an autoimmune condition such as Sj\u00f6gren syndrome. This review addresses the various causes of acquired sensory neuronopathies, the recommended diagnostic approach, and treatment options. Finally, I will briefly discuss a select few hereditary and degenerative sensory neuronopathies, which, in contrast to the acquired disorders, are slowly progressive and are usually associated with additional neurological symptoms. <jats:italic>Muscle Nerve<\/jats:italic> <jats:bold>53<\/jats:bold>: 8\u201319, 2016<\/jats:p>","DOI":"10.1002\/mus.24943","type":"journal-article","created":{"date-parts":[[2015,10,15]],"date-time":"2015-10-15T09:09:05Z","timestamp":1444900145000},"page":"8-19","source":"Crossref","is-referenced-by-count":86,"title":["Sensory neuronopathies"],"prefix":"10.1002","volume":"53","author":[{"given":"Kelly Graham","family":"Gwathmey","sequence":"first","affiliation":[{"name":"Department of Neurology University of Virginia P.O. 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