Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum

Neuroscience Letters

Volumn 441, Issue 1, 2008, Pages 21-24

  Chen, Qin ^a   Lui, Su ^a   Wang, Jian Gang ^a   Ou Yang, Luo ^b   Zhou, Dong ^a   Burgunder, Jean Marc ^a,c   Gong, Qi Yong ^a,d   Shang, Hui Fang ^a  

^a SICHUAN UNIVERSITY   (China)

^b SOUTHWEST UNIVERSITY   (China)

^c UNIVERSITY OF BERN   (Switzerland)

^d UNIVERSITY OF LIVERPOOL   (United Kingdom)

Author keywords

Diffusion tensor imaging (DTI); Fractional anisotropy (FA); Hereditary spastic paraplegia; Mean diffusion (MD); Thin corpus callosum; Voxel based analysis (VBA)

Indexed keywords

MUSCLE PROTEIN; PROTEIN SPATACSIN;

ADOLESCENT; ADULT; ARTICLE; BRAIN STEM; CAPSULA INTERNA; CASE REPORT; CEREBELLUM; CHINESE; CLINICAL FEATURE; CONTROLLED STUDY; CORPUS CALLOSUM; DIFFUSION TENSOR IMAGING; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; LABORATORY TEST; MALE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; THALAMUS; WHITE MATTER;

ADULT; BRAIN MAPPING; CORPUS CALLOSUM; DIFFUSION MAGNETIC RESONANCE IMAGING; HUMANS; MALE; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 46149098870     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2008.05.114     Document Type: Article

References (24)

1. Abe O., Yamada H., Masutani Y., Aoki S., Kunimatsu A., Yamasue H., Fukuda R., Kasai K., Hayashi N., Masumoto T., Mori H., Soma T., and Ohtomo K. Amyotrophic lateral sclerosis: diffusion tensor tractography and voxel-based analysis. NMR Biomed. 17 (2004) 411-416
2. Casali C., Valente E.M., Bertini E., Montagna G., Criscuolo C., De M.G., Villanova M., Damiano M., Pierallini A., Brancati F., Scarano V., Tessa A., Cricchi F., Grieco G.S., Muglia M., Carella M., Martini B., Rossi A., Amabile G.A., Nappi G., Filla A., Dallapiccola B., and Santorelli F.M. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 62 (2004) 262-268
3. Dreha-Kulaczewski S., Dechent P., Helms G., Frahm J., Gartner J., and Brockmann K. Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI. Neuroradiology 48 (2006) 893-898
4. Fink J.K. Hereditary spastic paraplegia. Neurol. Clin. 20 (2002) 711-726
5. Friston K., Ashburner J.J., Frith J.D., Poline J.B., Heather J.D., and Frackowiak R.S. Spatial registration and normalization of images. Hum. Brain Mapp. 3 (1995) 165-189
6. Friston K.J., Holmes A.P., Worsley K.J., Poline J.B., Frith J.D., and Frackowiak R.S. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Mapp. 2 (1995) 189-210
7. Kanaan R.A., Kim J.S., Kaufmann W.E., Pearlson G.D., Barker G.J., and McGuire P.K. Diffusion tensor imaging in schizophrenia. Biol. Psychiatry. 58 (2005) 921-929
8. Krabbe K., Nielsen J.E., Fallentin E., Fenger K., and Herning M. MRI of autosomal dominant pure spastic paraplegia. Neuroradiology 39 (1997) 724-727
9. Lossos A., Stevanin G., Meiner V., Argov Z., Bouslam N., Newman J.P., Gomori J.M., Klebe S., Lerer I., Elleuch N., Silverstein S., Durr A., Abramsky O., Ben-Nariah Z., and Brice A. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity. Arch. Neurol. 63 (2006) 756-760
10. Nakamura A., Izumi K., Umehara F., Kuriyama M., Hokezu Y., Nakagawa M., Shimmyozu K., Izumo S., and Osame M. Familial spastic paraplegia with mental impairment and thin corpus callosum. J. Neurol. Sci. 131 (1995) 35-42
11. Ohnishi J., Tomoda Y., and Yokoyama K. Neuroradiological findings in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol. Scand. 104 (2001) 191-192
12. Okubo S., Ueda M., Kamiya T., Mizumura S., Terashi A., and Katayama Y. Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol. Scand. 102 (2000) 196-199
13. Orlacchio A., Kawarai T., Totaro A., Errico A., St George-Hyslop P.H., Rugarli E.I., and Bernardi G. Hereditary spastic paraplegia: clinical genetic study of 15 families. Arch. Neurol. 61 (2004) 849-855
14. Pierpaoli C., Jezzard P., Basser P.J., Barnett A., and Di Chiro G. Diffusion tensor MR imaging of the human brain. Radiology 201 (1996) 637-648
15. Rosas H.D., Tuch D.S., Hevelone N.D., Zaleta A.K., Vangel M., Hersch S.M., and Salat D.H. Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures. Mov Disord. 21 (2006) 1317-1325
16. Rugg-Gunn F.J., Eriksson S.H., Symms M.R., Barker G.J., Thom M., Harkness W., and Duncan J.S. Diffusion tensor imaging in refractory epilepsy. Lancet 359 (2002) 1748-1751
17. Shibasaki Y., Tanaka H., Iwabuchi K., Kawasaki S., Kondo H., Uekawa K., Ueda M., Kamiya T., Katayama Y., Nakamura A., Takashima H., Nakagawa M., Masuda M., Utsumi H., Nakamuro T., Tada K., Kurohara K., Inoue K., Koike F., Sakai T., Tsuji S., and Kobayashi H. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15. Ann. Neurol. 48 (2000) 108-112
18. Simpson M.A., Cross H., Proukakis C., Pryde A., Hershberger R., Chatonnet A., Patton M.A., and Crosby A.H. Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. Am. J. Hum. Genet. 73 (2003) 1147-1156
19. Thivard L., Adam C., Hasboun D., Clemenceau S., Dezamis E., Lehericy S., Dormont D., Chiras J., Baulac M., and Dupont S. Interictal diffusion MRI in partial epilepsies explored with intracerebral electrodes. Brain 129 (2006) 375-385
20. Wakabayashi K., Kobayashi H., Kawasaki S., Kondo H., and Takahashi H. Autosomal recessive spastic paraplegia with hypoplastic corpus callosum, multisystem degeneration and ubiquitinated eosinophilic granules. Acta. Neuropathol. (Berl.) 101 (2001) 69-73
21. Weller S., and Gartner J. Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): mutations in the L1CAM gene. Hum. Mutat. 18 (2001) 1-12
22. Werring D.J., Clark C.A., Barker G.J., Thompson A.J., and Miller D.H. Diffusion tensor imaging of lesions and normal-appearing white matter in multiple sclerosis. Neurology 52 (1999) 1626-1632
23. Winner B., Uyanik G., Gross C., Lange M., Schulte-Mattler W., Schuierer G., Marienhagen J., Hehr U., and Winkler J. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). Arch. Neurol. 61 (2004) 117-121
24. Zhang S., Chen Q., Chen X., Wang J., Burgunder J., Yang Y., and Shang H.F. Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. Mov. Disord. 23 (2008) 917-919