Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome
Open Access
- 1 September 2000
- journal article
- case report
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 69 (3) , 392-395
- https://doi.org/10.1136/jnnp.69.3.392
Abstract
Senile chorea is a well recognised but poorly understood clinical entity characterised by a slowly progressive, generalised chorea in elderly people without mental deterioration or a clear underlying cause. The Hallervorden-Spatz syndrome is typically thought of as a paediatric condition with extrapyramidal features and dementia. However, it has been described in adults usually presenting with parkinsonism plus dementia. An elderly woman with slowly progressive chorea without dementia was found at postmortem to have the pathological features originally described by Hallervorden and Spatz. This association has not previously been reported.Keywords
This publication has 9 references indexed in Scilit:
- Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13Nature Genetics, 1996
- Naming of syndromes and unethical activities: the case of Hallervorden and SpatzThe Lancet, 1996
- Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease.Journal of Neurology, Neurosurgery & Psychiatry, 1996
- A case of senile choreaMovement Disorders, 1990
- Late onset parkinsonian syndrome in Hallervorden-Spatz disease.Journal of Neurology, Neurosurgery & Psychiatry, 1987
- ADULT ONSET HALLERVORDEN-SPATZ DISEASE WITH NEUROFIBRILLARY PATHOLOGYBrain, 1987
- Late‐onset Hallervorden‐Spatz disease presenting as familial parkinsonismNeurology, 1985
- Hallervorden-Spatz SyndromeArchives of Neurology, 1974
- Unusual late-onset type of Hallervorden-Spatz diseaseZeitschrift für Neurologie, 1972