CareLit Fachartikel

MRI and Electrophysiological Characterization of Patients Suffering from Pure and Complicated Hereditary Spastic Paraplegia

J Kassubek, AD Sperfeld · Klinische Neurophysiologie · 2004 · Heft 08

Dokument
1162311
CareLit-ID
Jahr
2004
Publikation
PDF
nein
Metadaten
DOI
ja
zitierfähig

Bibliografische Angaben

Zeitschrift
Klinische Neurophysiologie
Autor:innen
J Kassubek, AD Sperfeld
Ausgabe
Heft 08 / 2004
Seiten
–
Erschienen: 2004-08-25 00:00:00
ISSN
1434-0275

Zusammenfassung

Hereditary spastic paraplegia (HSP) is a phenotypically and genotypically heterogeneous neurodegenerative disease encompassing a group of disorders mainly characterized by spastic paraparesis of the lower limbs. From the clinical point of view, HSP can be classified into complicated and pure forms. The present study contains clinical, magnetic resonance imaging (MRI), and electrophysiological investigations of a total of 33 HSP patients suffering from pure (n=22) and complicated forms (n=11), respectively. The MRI standard protocol was performed both for the brain (including a volume-rendering MP-RAGE data set,…

Schlagworte

Corpus Callosum Atrophy Klinische Neurophysiologie