References
Jones HR Jr, Hedley-Whyte ET (1983) Idiopathic haemochromatosis (IHC): dementia and ataxia as presenting signs. Neurology 33:1479–1483
Schröder J, Haan J (1987) Extrapyramidales syndrom bei idiopathischer heämochromatose (IHC). Nervenarzt 58:577–578
Nielsen J E, Neerup Jensen L, Krabbe K (1995) Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. J Neurol Neurosurg Psychiatry 59:318–321
Harvey RJ, Summerfield JA, Fox NC, Warrington EK, Rossor MN (1997) Dementia associated with haemochromatosis: a report of two cases. Eur J Neurol 4:318–322
Demarquay G, Setiey A, Morel Y, Trepo C, Chazot G, Broussolle E (2000) Clinical report of three patients with hereditary hemochromatosis and movement disorders. Mov Disord 15:1204–1209
Dethy S, Caroyer J-M (2004) Reversible parkinsonism associated with haemochromatosis. Mov Disord 19(Suppl 9):S327–348, P951
Costello DJ, Walsh SL, Harrington HJ, Walsh CH (2004) Concurrent hereditary haemochromatosis and idiopathic Parkinson’ disease: a case report series. J Neurol Neurosurg Psychiatry 75:631–633
Russo N, Edwards M, Andrews T, O’Brien M, Bhatia KP (2004) Hereditary hemochromatosis is unlikely to cause movement disorders. J Neurol 251:849–852
Demarquay G, Thobois S, Latour P, Broussolle E (2006) Hereditary haemochromatosis and movement disorders: the still controversial relationship. J Neurol 253:261–262
Berg D, Hoggenmüller U, Hofmann E, Fischer R, Kraus M, Scheurlen M, Becker G (2000) The basal ganglia in haemochromatosis. Neuradiology 42:9–13
Datz C, Haas T, Rinner H, Sandhofer F, Patsch W, Paulweber B (1998) Heterozygosity for the C282Y mutation in the haemochromatosis gene is associated with increased serum iron, transferring saturation, and hemoglobin in young women: a protective role against iron deficiency? Clin Chem 44:2429–2432
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Rutgers, M.P., Pielen, A. & Gille, M. Chronic cerebellar ataxia and hereditary hemochromatosis: causal or coincidental association?. J Neurol 254, 1296–1297 (2007). https://doi.org/10.1007/s00415-006-0507-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00415-006-0507-2