Abstract
AbstractWe describe the case of a 51‐year‐old woman with Krabbe disease presenting with progressive spastic paraparesis since she was 10 years‐of‐age. At the age of 51 years, neurological evaluation showed progression of her sensorimotor neuropathy along with deterioration of nerve conduction, whereas no apparent progression of the bilateral pyramidal tract lesions was observed by magnetic resonance imaging. Sensorimotor neuropathy progresses over several decades in its long‐term natural course in contrast to the absence of apparent progression of lesions in the central motor pathways.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.