Literature DB >> 18678379

Serum vitamin B12 deficiency and hyperhomocystinemia: a reversible cause of acute chorea, cerebellar ataxia in an adult with cerebral ischemia.

C Shyambabu1, S Sinha, A B Taly, J Vijayan, J M E Kovoor.   

Abstract

Patients with vitamin B12 deficiency have protean neurological manifestations that are often insidious. Acute onset of cerebellar dysfunction and extrapyramidal manifestations like dystonia and chorea are rather uncommon in adults. We describe a patient who manifested with acute onset of language dysfunction, chorea and ataxia. There was no history of hypertension, diabetes or ischemic heart disease. He had low serum vitamin B12 and elevated serum homocystine levels. He improved dramatically following B12 replacement therapy. Our patient provides insight into the pathophysiological mechanism of this rare manifestation. Further the importance of considering vitamin B12 deficiency, in country like India, where vegetarian food practice is quite common, is being emphasized.

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Year:  2008        PMID: 18678379     DOI: 10.1016/j.jns.2008.06.034

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  4 in total

1.  Reversible parkinsonism and cognitive deficits due to vitamin B₁₂ deficiency.

Authors:  Ana Filipa Santos; Margarida Rodrigues; Pedro Abreu; Carla Ferreira
Journal:  Neurol Sci       Date:  2015-03-04       Impact factor: 3.307

Review 2.  Diagnosis and treatment of chorea syndromes.

Authors:  Andreas Hermann; Ruth H Walker
Journal:  Curr Neurol Neurosci Rep       Date:  2015       Impact factor: 5.081

Review 3.  Differential diagnosis of chorea.

Authors:  Ruth H Walker
Journal:  Curr Neurol Neurosci Rep       Date:  2011-08       Impact factor: 5.081

4.  Left-Hand Motor Stereotypy in Vitamin B12 Deficiency: Expanding the Spectrum of Infantile Tremor Syndrome.

Authors:  Divyani Garg; Suvasini Sharma; Sanjay Pandey
Journal:  Ann Indian Acad Neurol       Date:  2020-04-07       Impact factor: 1.383

  4 in total

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