This is a preview of subscription content, log in via an institution to check access.
References
Casali C, Valente EM, Bertini E, et al. (2004) Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 62:262–268
Coutinho P, Barros J, Zemmouri R, et al. (1999) Clinical heterogeneity of autosomal recessive spastic paraplegias. Arch Neurol 56:943–949
Dupre N, Howard HC, Mathieu J, et al. (2003) Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol 54:9–18
Farah S, Sabry MA, Al-Shubaili AFK, et al. (1997) Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: new entity? Clin Neurol Neurosurg 99:66–70
Fink JK (2002) Hereditary spastic paraplegia: the pace quickens. Ann Neurol 51:669–672
Fink JK (2003) The Hereditary Spastic Paraplegias. Arch Neurol 60:1045–1049
Harding AE (1990) The hereditary ataxias and paraplegias. In: Emery AEH, Rimoin DL (eds) Principles and Practice of Medical Genetics. London: Churchill Livingstone, pp 383–396
Kantarci M, Ertas U, Alper F, et al. (2003) Gorlin’s syndrome with a thin copus callosum and a third ventricular cyst. Diagn Neuroradiol 234:1–5
Kobayashi H, Garcia CA, Alfonso G, et al. (1996) Molecular genetics of familial spastic paraplegia: a multitude of responsible genes. J Neurol Sci 137:131–138
McDermott CJ, White K, Bushby K, et al. (2000) Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69:150–160
Nakamura A, Izumi K, Umehara F, et al. (1995) Familial spastic paraplegia with mental impairment and thin corpus callosum. J Neurol Sci 131:35–42
Patel H, Cross H, Proukakis C, et al. (2002) SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nature Genetics 31:347–348
Simpson MA, Cross H, Proukakis C, et al. (2003) Maspardin is mutated in MAST syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. Am J Hum Genet 73:1147–1156
Winner B, Uyanik G, Gross C, et al. (2004) Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). Arch Neurol 61:117–121
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Sperfeld, AD., Kassubek, J., Crosby, A.H. et al. Complicated hereditary spastic paraplegia with thin corpus callosum: Variation of phenotypic expression over time. J Neurol 251, 1285–1287 (2004). https://doi.org/10.1007/s00415-004-0562-5
Received:
Revised:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/s00415-004-0562-5