Pallido-nigro-luysial atrophy associated with degeneration of the centrum medianum
- 1 January 1977
- journal article
- research article
- Published by Springer Nature in Acta Neuropathologica
- Vol. 37 (1) , 81-85
- https://doi.org/10.1007/bf00684546
Abstract
A 66-year-old man (case 1) and a 71-year-old woman (case 2) showed systemic degeneration of the globus pallidus, substancia nigra, subthalamic nucleus, centrum medianum thalami and at times, superior colliculus in the midbrain. In the pallido-nigral system, neuronal loss was severe in both cases and an increase of pigment and granular spheroids was marked in case 2, less in case 1. Electron-microscopilly, the spheroids consisted of aggregates of highly dense material, often membrane-bound, and varying amounts of groups of loosely packed filaments. Clinical symptoms were stereotyped and unique, showing severe akinesia, no rigidity in the limbs, no tremor but retropulsions, upward gaze palsy, dysarthria, dysphagia and later, nuchal stiffness. Nosological identification is discussed.This publication has 11 references indexed in Scilit:
- Infantile neuroaxonal dystrophy: Cortical axonic and presynaptic changesActa Neuropathologica, 1970
- La dystrophie neuroaxonale infantile ou maladie de SeitelbergerActa Neuropathologica, 1970
- Progressive pallidumatrophieJournal of the Neurological Sciences, 1968
- ?Striato-nigrale Degeneration?Acta Neuropathologica, 1968
- Clinico-Pathological and Histochemical Studies of Hallervorden-Spatz Disease with Torsion Dystonia with Special Reference to Diagnostic Criteria of the Disease from the Clinico-Pathological ViewpointPublished by Elsevier ,1966
- Progressive Supranuclear PalsyArchives of Neurology, 1964
- Beitrag zur spätinfantilen Hallervorden-Spatzschen KrankheitActa Neuropathologica, 1963
- IX. Sur une affection hérédo-familiale apparentée à Ia maladie d'Hallervorden-Spatz et aux atrophies cérébelleuses, caracterisée par un syndrome cérébello-myoclonique évoluant lentement et tardivement vers un état rigide au cours d'une neurofibromatose; pp. 183–197European Neurology, 1947
- ASPECTS CLINIQUES ET PATHOLOGIQUES DES ATROPHIES PALLIDALES ET PALLIDO-LUYSIENNES PROGRESSIVESJournal of Neurology, Neurosurgery & Psychiatry, 1946
- A SYSTEM DISEASE OF THE PARALYSIS AGITANS TYPE, CHARACTERIZED BY ATROPHY OF THE MOTOR CELLS OF THE CORPUS STRIATUMBrain, 1917