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- Edina Vitaszil, Ilona Jelencsik, and Imre Szirmai.
- Semmelweis Egyetem, Neurológiai Klinika, H-1083 Budapest, Balassa u. 6.
- Ideggyogy Szemle. 2002 Nov 20; 55 (11-12): 382-93.
AbstractThe clinical diagnosis of inherited spinocerebellar ataxias is difficult, because phenotypes frequently overlap. The authors attempt to review the different inherited ataxia syndromes, discussing the most frequent one, Friedreich-ataxia in detail. The case of a patient with Friedreich-ataxia is presented, where the genetically supported diagnosis has been made more than ten years following the onset of the symptoms, after several hospitalizations and misdiagnosis. The correct diagnosis can be established based on the Geoffroy-Harding criteria and gene mutation analysis.
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