MR imaging findings in autosomal recessive hereditary spastic paraplegia

American Journal of Neuroradiology

Volumn 30, Issue 5, 2009, Pages 936-940

  Hourani, Roula ^a   El Hajj, T ^a   Barada, W H ^a   Hourani, M ^a   Yamout, B I ^a  

^a AMERICAN UNIVERSITY OF BEIRUT   (Lebanon)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN; BRAIN ATROPHY; CAPSULA INTERNA; CLINICAL ARTICLE; CORPUS CALLOSUM; DIAGNOSTIC IMAGING; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LEBANON; MALE; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PYRAMIDAL TRACT; SIGNAL TRANSDUCTION; SPINAL CORD ATROPHY; SPINE; WHITE MATTER;

ADULT; BRAIN; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; SPASTIC PARAPLEGIA, HEREDITARY; SPINAL CORD; YOUNG ADULT;

EID: 65949116827     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: 10.3174/ajnr.A1483     Document Type: Article

References (36)

1. Keppen LD, Leppert MF, O'Connell P, et al. Etiological heterogeneity in X-linked spastic paraplegia. Am J Hum Genet 1987;41:933-943 (Pubitemid 18108148)
2. Goldblatt J, Ballo R, Sachs B, et al. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype. Clin Genet 1989;35:116-120 (Pubitemid 19062300)
3. Durr A, Brice A, Serdaru M, et al. The phenotype of "pure" autosomal dominant spastic paraplegia. Neurology 1994;44:1274-1277 (Pubitemid 24232228)
4. Hedera P, Eldevik OP, Maly P, et al. Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia. Neuroradiology 2005;47:730-734 (Pubitemid 41554553)
5. Lesca G, Eymard-Pierre E, Santorelli FM, et al. Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families. Neurology 2003;60:674-682 (Pubitemid 36246088)
6. Marti-Fabregas J, Pujol J. Selective involvement of the pyramidal tract on magnetic resonance imaging in primary lateral sclerosis. Neurology 1990;40:1799-1800 (Pubitemid 20383157)
7. Krabbe K, Nielsen JE, Fallentin E, et al. MRI of autosomal dominant pure spastic paraplegia. Neuroradiology 1997;39:724-727 (Pubitemid 27425067)
8. 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
9. Kuru S, Sakai M, Konagaya M, et al. Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter. Neuropathology 2005;25:346-352 (Pubitemid 43943244)
10. Nicolau A, Diard F, Fontan D, et al. Magnetic resonance imaging in spinocerebellar degenerative diseases (apropos of 8 cases) [in French]. Pediatrie 1987;42:359-365
11. Harding AE. Hereditary "pure" spastic paraplegia. In: Harding A, ed. The Hereditary Ataxias and Related Disorders. Edinburgh, UK: Churchill Livingstone; 1984:191-213
12. 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;56:943-949 (Pubitemid 29374811)
13. Bruyn RP. The neuropathology of hereditary spastic paraparesis. Clin Neurol Neurosurg 1992;94(suppl):S16-18
14. Nomura H, Koike F, Tsuruta Y, et al. Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology. Neuropathology 2001;21:212-217 (Pubitemid 32947284)
15. 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;251:1105-1110 (Pubitemid 39297207)
16. Kassubek J, Sperfeld AD, Baumgartner A, et al. Brain atrophy in pure and complicated hereditary spastic paraparesis: a quantitative 3D MRI study. Eur J Neurol 2006;13:880-886 (Pubitemid 44124686)
17. Gilman S, Manter JT, Gatz AJ. Manter and Gatz's Essentials of Clinical Neuroanatomy and Neurophysiology. F.A. Davis Co; 2002:181
18. Ormerod IE, Harding AE, Miller DH, et al. Magnetic resonance imaging in degenerative ataxic disorders. J Neurol Neurosurg Psychiatry 1994;57:51-57 (Pubitemid 24030908)
19. 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;52:665-669
20. Teive HA, Iwamoto FM, Della Coletta MV, et al. Hereditary spastic paraplegia associated with thin corpus callosum. Arq Neuropsiquiatr 2001;59:790-792 (Pubitemid 33607236)
21. 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;102:196-199 (Pubitemid 30645139)
22. Ferrer I, Olive M, Rivera R, et al. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy: a neuropathological study. Neuropathol Appl Neurobiol 1995;21:255-261
23. Orlacchio A, Kawarai T, Totaro A, et al. Hereditary spastic paraplegia: clinical genetic study of 15 families. Arch Neurol 2004;61:849-855 (Pubitemid 38747323)
24. Alber B, Pernauer M, Schwan A, et al. Spastin related hereditary spastic paraplegia with dysplastic corpus callosum. J Neurol Sci 2005;236:9-12 (Pubitemid 41218686)
25. 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;251:1285-1287 (Pubitemid 39517939)
26. Auer-Grumbach M, Fazekas F, Radner H, et al. Troyer syndrome: a combination of central brain abnormality and motor neuron disease? J Neurol 1999;246:556-561 (Pubitemid 29376280)
27. Casali C, Valente EM, Bertini E, et al. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 2004;62:262-268 (Pubitemid 38167136)
28. Somasundaram S, Raghavendra S, Singh A., et al. Hereditary spastic paraplegia with a thin corpus callosum. Pediatr Radiol 2007;37:503-505 (Pubitemid 46567103)
29. Dreha-Kulaczewski S, Dechent P, Helms G, et al. Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI. Neuroradiology 2006;48:893-898
30. 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;44:371-381 (Pubitemid 36097186)
31. 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;61:117-121 (Pubitemid 38067422)
32. Ohnishi J, Tomoda Y, Yokoyama K. Neuroradiological findings in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol Scand 2001;104:191-192 (Pubitemid 32831785)
33. Sperfeld AD, Baumgartner A, Kassubek J. Magnetic resonance investigation of the upper spinal cord in pure and complicated hereditary spastic paraparesis. Eur Neurol 2005;54:181-185
34. Sperfeld AD, Bretschneider V, Flaith L, et al. MR-pathologic comparison of the upper spinal cord in different motor neuron diseases. Eur Neurol 2005;53:74-77 (Pubitemid 40868705)
35. 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 (Pubitemid 28156539)
36. 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