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Fig. 1 | BMC Neurology

Fig. 1

From: A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Fig. 1

Brain MRI of the patient F83–581. a Sagittal T1 section showing thinning in the isthmus of the corpus callosum (arrow). b and c Axial T1 section showing periventricular white matter changes and scattered hyperintensities in the white matter, cerebellum, and right side of the pons (arrows). The cerebrum, brain stem, and cerebellum were not atrophied

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BMC Neurology

ISSN: 1471-2377

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