The neuropathology of hereditary spastic paraparesis.

Clin Neurol Neurosurg

Department of Neurology, Oudenrijn Hospital, Utrecht, The Netherlands.

Published: August 1992

AI Article Synopsis

Article Abstract

Hereditary spastic paraparesis or Strümpell's disease is a genetically determined neurodegenerative disorder in which the signs and symptoms are predominant in the legs. Inheritance is usually autosomal dominant and in a minority recessive. Neuropathological study reveals a degeneration of the corticospinal tract decreasing from lower lumbar to cervical level and of posterior columns increasing from lumbar to upper cervical level as well as degeneration of the spinocerebellar tracts in approximately 50%. The nature of this nucleo-distal central axonopathy and clinicopathological discrepancy for posterior columns, as well as the limits of the pathological process are poorly understood.

Download full-text PDF

Source
http://dx.doi.org/10.1016/0303-8467(92)90010-zDOI Listing

Publication Analysis

Top Keywords

hereditary spastic
8
spastic paraparesis
8
cervical level
8
posterior columns
8
neuropathology hereditary
4
paraparesis hereditary
4
paraparesis strümpell's
4
strümpell's disease
4
disease genetically
4
genetically determined
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!