Abstract
Summary Morphological features of the central nervous system, by light and electron microscopy, are reported in various encephalopathies by inborn enzymatic defect in lipid, glucidic and aminoacid metabolisms. The authors stress on the caracteristics of the abnormal storage material in Neurolipidoses, Ceroid-Lipofuscinoses, Glycogenosis type II and Lafora disease. On the other hand, they insist on the non specific lesions of the central nervous system in Aminoacidopathies by enzymatic defect.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Revue d'Électroencéphalographie et de Neurophysiologie Clinique
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.
