Computerized tomography in hereditary ataxias
- 29 January 2009
- journal article
- research article
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 58 (2) , 81-88
- https://doi.org/10.1111/j.1600-0404.1978.tb02864.x
Abstract
Patients [39] with hereditary ataxia (HA), hereditary spastic paraplegia or Charcot-Marie-Tooth disease were investigated with computerized cranial tomography (CT). Infratentorial as well as supratentorial atrophies were registered and scored. These were compared with the patient''s neurological symptoms, which were related to the lesion in the CNS and scored. There was correlation between the distribution of brainstem/cerebellar symptoms and the distribution and degree of infratentorial atrophy. HA cases with cerebral cortical atrophy had significantly higher dementia scores than those without wide sulci. I.v. injection with contrast medium was of no diagnostic aid, as no focal changes were found. CT is an aid in the diagnosis of hereditary ataxias and hereditary spastic paraplegia.This publication has 16 references indexed in Scilit:
- Cranial Computerized Tomography and Marie's AtaxiaArchives of Neurology, 1978
- Adult-Onset Hereditary Ataxia in ScotlandArchives of Neurology, 1977
- C.A.T. in Leukodystrophy and Neuronal DegenerationPublished by Springer Nature ,1977
- The clinical significance of pneumographic cerebellar atrophyThe British Journal of Radiology, 1976
- PNEUMOENCEPHALOGRAPHIC FINDINGS IN VARIOUS PRIMARY and SECONDARY MUSCULAR DISORDERSActa Neurologica Scandinavica, 1976
- Computer tomography of the cerebrum in multiple sclerosisNeuroradiology, 1976
- THE OLIVOPONTOCEREBELLAR ATROPHIESMedicine, 1970
- HEREDITARY SPASTIC PARAPLEGIA. A Family with Ten InjuredActa Psychiatrica Scandinavica, 1959
- FORMS OF FAMILIAL ATAXIA RESEMBLING MULTIPLE SCLEROSISArchives of Neurology & Psychiatry, 1937
- Ueber Ataxie mit besonderer Berücksichtigung der hereditären FormenVirchows Archiv, 1876