The neuropathological features of neuroacanthocytosis
- 1 January 1994
- journal article
- case report
- Published by Wiley in Movement Disorders
- Vol. 9 (3) , 297-304
- https://doi.org/10.1002/mds.870090303
Abstract
In this article we describe the neuropathological changes in three patients with neuroacanthocytosis and review the neuropathology of the other eight cases reported in the literature. Macroscopically the brains showed enlargement of the lateral ventricles, especially the frontal horns. The most severely and consistently affected brain areas were the caudate nucleus and putamen, which were atrophic and showed by light microscopy marked neuronal loss and gliosis. Small and medium‐sized striatal neurons were particularly depleted. The globus pallidus was almost as severely involved as the striatum. In some cases the thalamus, substantia nigra, and anterior horns of the spinal cord showed pathology, mainly neuronal loss and mild gliosis. Brain areas with no pathology included the subthalamic nucleus, cerebral cortex, cerebellum, pons, and medulla. The preservation of these areas may help in the neuropathological distinction of neuroacanthocytosis from Huntington's disease.Keywords
This publication has 41 references indexed in Scilit:
- Turning off cortical ensembles stops striatal Up states and elicits phase perturbations in cortical and striatal slow oscillations in rat in vivoThe Journal of Physiology, 2006
- Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: A positron emission tomographic studyAnnals of Neurology, 1991
- D 1 and D 2 Dopamine Receptor-regulated Gene Expression of Striatonigral and Striatopallidal NeuronsScience, 1990
- Third Dorothy S. Russell Memorial Lecture: Huntington's disease: some recent neuropathological studiesNeuropathology and Applied Neurobiology, 1990
- Neurochemical findings in neuroacanthocytosisMovement Disorders, 1988
- Neuropathological study of chorea-acanthocytosis.Japanese Journal of Medicine, 1984
- Neurogenic muscular atrophy and low density of large myelinated fibres of sural nerve in chorea-acanthocytosis.Journal of Neurology, Neurosurgery & Psychiatry, 1981
- Familial degeneration of the basal ganglia with acanthocytosis: A clinical, neuropathological, and neurochemical studyAnnals of Neurology, 1978
- A case of striatal hemiplegia.Journal of Neurology, Neurosurgery & Psychiatry, 1967
- A New Phenotype (McLeod) in the Kell Blood‐group System*Vox Sanguinis, 1961