Research ArticleBRAIN
MR Imaging Findings in Autosomal Recessive Hereditary Spastic Paraplegia
R. Hourani, T. El-Hajj, W.H. Barada, M. Hourani and B.I. Yamout
American Journal of Neuroradiology May 2009, 30 (5) 936-940; DOI: https://doi.org/10.3174/ajnr.A1483
R. Hourani
T. El-Hajj
W.H. Barada
M. Hourani

References
- ↵Keppen LD, Leppert MF, O'Connell P, et al. Etiological heterogeneity in X-linked spastic paraplegia. Am J Hum Genet 1987;41:933–43
- ↵Goldblatt J, Ballo R, Sachs B, et al. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype. Clin Genet 1989;35:116–20
- ↵Durr A, Brice A, Serdaru M, et al. The phenotype of “pure” autosomal dominant spastic paraplegia. Neurology 1994;44:1274–77
- ↵Hedera P, Eldevik OP, Maly P, et al. Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia. Neuroradiology 2005;47:730–34
- ↵Lesca G, Eymard-Pierre E, Santorelli FM, et al. Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families. Neurology 2003;60:674–82
- Marti-Fabregas J, Pujol J. Selective involvement of the pyramidal tract on magnetic resonance imaging in primary lateral sclerosis. Neurology 1990;40:1799–800
- ↵Krabbe K, Nielsen JE, Fallentin E, et al. MRI of autosomal dominant pure spastic paraplegia. Neuroradiology 1997;39:724–27
- ↵Nakamura A, Izumi K, Umehara F, et al. Familial spastic paraplegia with mental impairment and thin corpus callosum. J Neurol Sci 1995;131:35–42
- ↵
- ↵Nicolau A, Diard F, Fontan D, et al. Magnetic resonance imaging in spinocerebellar degenerative diseases (apropos of 8 cases) [in French]. Pediatrie 1987;42:359–65
- ↵Harding AE. Hereditary “pure” spastic paraplegia. In: Harding A, ed. The Hereditary Ataxias and Related Disorders. Edinburgh, UK: Churchill Livingstone;1984 :191–213
- ↵Coutinho P, Barros J, Zemmouri R, et al. Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families. Arch Neurol 1999;56:943–49
- ↵Bruyn RP. The neuropathology of hereditary spastic paraparesis. Clin Neurol Neurosurg 1992;94 (suppl):S16–18
- Nomura H, Koike F, Tsuruta Y, et al. Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology. Neuropathology 2001;21:212–17
- ↵Proukakis C, Cross H, Patel H, et al. Troyer syndrome revisited: a clinical and radiological study of a complicated hereditary spastic paraplegia. J Neurol 2004;251:1105–10
- ↵
- ↵Gilman S, Manter JT, Gatz AJ. Manter and Gatz's Essentials of Clinical Neuroanatomy and Neurophysiology. F.A. Davis Co;2002 :181
- ↵Ormerod IE, Harding AE, Miller DH, et al. Magnetic resonance imaging in degenerative ataxic disorders. J Neurol Neurosurg Psychiatry 1994;57:51–57
- ↵Cambi F, Tartaglino L, Lublin F, et al. X-linked pure familial spastic paraparesis: characterization of a large kindred with magnetic resonance imaging studies. Arch Neurol 1995;52:665–69
- ↵Teive HA, Iwamoto FM, Della Coletta MV, et al. Hereditary spastic paraplegia associated with thin corpus callosum. Arq Neuropsiquiatr 2001;59:790–92
- ↵Okubo S, Ueda M, Kamiya T, et al. Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol Scand 2000;102:196–99
- ↵Ferrer I, Olive M, Rivera R, et al. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy: a neuropathological study. Neuropathol Appl Neurobiol 1995;21:255–61
- ↵Orlacchio A, Kawarai T, Totaro A, et al. Hereditary spastic paraplegia: clinical genetic study of 15 families. Arch Neurol 2004;61:849–55
- ↵
- ↵Sperfeld AD, Kassubek J, Crosby AH, et al. Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time. J Neurol 2004;251:1285–87
- ↵Auer-Grumbach M, Fazekas F, Radner H, et al. Troyer syndrome: a combination of central brain abnormality and motor neuron disease? J Neurol 1999;246:556–61
- ↵Casali C, Valente EM, Bertini E, et al. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 2004;62:262–68
- ↵
- ↵
- ↵Moller-Hartmann W, Herminghaus S, Krings T, et al. Clinical application of proton magnetic resonance spectroscopy in the diagnosis of intracranial mass lesions. Neuroradiology 2002;44:371–81
- ↵Winner B, Uyanik G, Gross C, et al. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus collasum in spastic gait gene 11 (SPG11). Arch Neurol 2004;61:117–21
- ↵Ohnishi J, Tomoda Y, Yokoyama K. Neuroradiological findings in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol Scand 2001;104:191–92
- ↵
- ↵
- ↵Nielsen JE, Krabbe K, Jennum P, et al. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study. J Neurol Neurosurg Psychiatry 1998;64:61–66
- ↵Hourani R, Barada W, El-Hajj T, et al. Posterior column atrophy in autosomal recessive hereditary spastic paraplegia: MRI finding. Eur J Radiol Extra 2008;65:37–68
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R. Hourani, T. El-Hajj, W.H. Barada, M. Hourani, B.I. Yamout
MR Imaging Findings in Autosomal Recessive Hereditary Spastic Paraplegia
American Journal of Neuroradiology May 2009, 30 (5) 936-940; DOI: 10.3174/ajnr.A1483
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