Title |
Chorea-acanthocytosis: a case report
|
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Published in |
International Medical Case Reports Journal, February 2016
|
DOI | 10.2147/imcrj.s95882 |
Pubmed ID | |
Authors |
Lekhjung Thapa, Suman Bhattarai, Milan P Shrestha, Rajesh Panth, Dinesh Nath Gongal, Upendra Prasad Devkota |
Abstract |
Neuroacanthocytosis is a group of rare disorders. We report a 36-year-old right-handed female who presented with gradually progressive abnormal facial movements, generalized weakness, and lower-lip biting starting 4 years ago. On examination, she had lower-lip ulcer, orofacial dyskinesias, and peripheral neuropathy. Her peripheral blood smears showed acanthocytosis and magnetic resonance imaging revealed atrophied head of caudate nuclei and putaminal hyperintensities on T2-weighted and fluid attenuated inversion recovery images. Work-up for autoimmune and metabolic causes was negative. She was diagnosed with chorea-acanthocytosis, an entity under neuroacanthocytosis syndrome and the patient was offered symptomatic treatment. |
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Geographical breakdown
Country | Count | As % |
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Unknown | 13 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Master | 2 | 15% |
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Student > Ph. D. Student | 1 | 8% |
Professor | 1 | 8% |
Other | 2 | 15% |
Unknown | 2 | 15% |
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Neuroscience | 1 | 8% |
Other | 0 | 0% |
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