Neuroacanthocytosis: A rare movement disorder with magnetic resonance imaging
In betalipoprotein deficiencies, lack of microsomal triglyceride transfer protein (MTP) or a direct mutation in the gene for betapolipoprotein leads to a decreased absorption of vitamin E as well as other vitamins and possibly other cofactors. The case discussed here gives us an important message, i...
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| Veröffentlicht in: | Journal of neurosciences in rural practice 2011-01, Vol.2 (1), p.111-112 |
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| container_title | Journal of neurosciences in rural practice |
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| creator | Gautam, G Hashmi, Ma Pandey, Arindam |
| description | In betalipoprotein deficiencies, lack of microsomal triglyceride transfer protein (MTP) or a direct mutation in the gene for betapolipoprotein leads to a decreased absorption of vitamin E as well as other vitamins and possibly other cofactors. The case discussed here gives us an important message, i.e., typical MRI imaging finding "eye-of-the-tiger" sign appearance with associated peripheral blood smear study showing acanthocytes is useful in detecting this rare neurological disease. |
| doi_str_mv | 10.4103/0976-3147.80078 |
| format | Article |
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| language | eng |
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| source | PubMed Central Open Access; Thieme Connect Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central |
| subjects | Apolipoproteins Ataxia Care and treatment Diagnosis Disease Health aspects Letters to the Editor Magnetic resonance imaging Medical research Movement disorders Peripheral nerve diseases Risk factors |
| title | Neuroacanthocytosis: A rare movement disorder with magnetic resonance imaging |
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