Abbreviations
- HA:
-
hereditary aceruloplasminemia
- HD:
-
Huntington’s disease
- HH:
-
hereditary hemochromatosis
- NBIA:
-
Neurodegenerations with Brain Iron Accumulation
- PKAN:
-
Pantothenate Kinase-Associated Neurodegeneration
References
Berg D, Hoggenmuller U, Hofmann E, Fischer R, Kraus M, Scheurlen M, Becker G (2000) The basal ganglia in haemochromatosis. Neuroradiology 42:9–13
Costello DJ, Walsh SL, Harrington HJ, Walsh CH (2004) Concurrent hereditary haemochromatosis and idiopathic Parkinson’s disease: a case report series. J Neurol Neurosurg Psychiatry 75:631–633
Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J (2001) Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nature Genet 28:350–354
Graham JM, Paley MN, Grunewald RA, Hoggard N, Griffiths PD (2000) Brain iron deposition in Parkinson’s disease imaged using the PRIME magnetic resonance sequence. Brain 123:2423–2431
Haba-Rubio J, Staner L, Petiau C, Erb G, Schunck T, Macher JP (2005) Restless legs syndrome and low brain iron levels in patients with haemochromatosis. J Neurol Neurosurg Psychiatry 76:1009–1010
Hayflick SJ (2003) Unraveling the Hallervorden-Spatz syndrome: pantothenate kinase-associated neurodegeneration is the name. Curr Opin Pediatr. 15:572–577
Kitzberger R, Madl C, Ferenci P (2005) Wilson disease Metab. Brain Dis 20:295–302
Mubaidin A, Roberts E, Hampshire D, Dehyyat M, Shurbaji A, Mubaidien M, Jamil A, Al-Din A, Kurdi A, Woods CG (2003) Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum. J Med Genet 40:543–546
Nielsen JE, Jensen LN, 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
Russo N, Edwards M, Andrews T, O’Brien M, Bhatia KP (2004) Hereditary haemochromatosis is unlikely to cause movement disorders - a critical review. J Neurol 251:849–852
Schroder J, Haan J (1987) Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures (CCT, MRT). Nervenarzt 58:577–578
Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, Morita H, Hiyamuta S, Ikeda S, Shimizu N, Yanagisawa N (1995) A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nat Genet 9:267–272
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Fasano, A., Bentivoglio, A.R. & Colosimo, C. Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis. J Neurol 254, 113–114 (2007). https://doi.org/10.1007/s00415-006-0289-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00415-006-0289-6