Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome
- 1 May 1994
- journal article
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 89 (5) , 347-352
- https://doi.org/10.1111/j.1600-0404.1994.tb02645.x
Abstract
An unusual neurological syndrome in an Arab family with five affected siblings, is reported. Autosomal recessive inheritance is suggested by having multiple affected siblings born to phenotypically normal consanguineous parents. Similar to Davison's Pallido-pyramidal syndrome, they presented with the clinical signs and symptoms of severe parkinsonism as well as evidence of cortico-spinal tract disease. In addition, they had dementia and supranuclear upgaze paresis. MRI studies showed significant atrophy of the globus pallidus and the pyramids, as well as generalized brain atrophy in later stages. Therapy with levodopa resulted in significant improvement in the extrapyramidal dysfunction. We suggest that this probably represents a new syndrome which is closely related but not identical to the pallido-pyramidal syndrome.Keywords
This publication has 16 references indexed in Scilit:
- Striatonigral degenerationNeurology, 1990
- The clinical features and natural history of the Steele‐Richardson‐Olszewski syndrome (progressive supranuclear palsy)Neurology, 1986
- Isolated Failure of Autonomic Noradrenergic NeurotransmissionNew England Journal of Medicine, 1986
- Late‐onset Hallervorden‐Spatz disease presenting as familial parkinsonismNeurology, 1985
- New form of familial Parkinson‐dementia syndromeNeurology, 1983
- Pallido-pyramidal syndrome treated with levodopa.Journal of Neurology, Neurosurgery & Psychiatry, 1975
- Report of Familial Cases of ParkinsonismJAMA, 1962
- A Neurological Syndrome Associated with Orthostatic HypotensionA.M.A. Archives of Neurology, 1960
- PALLIDO-PYRAMIDAL DISEASEJournal of Neuropathology and Experimental Neurology, 1954
- PROGRESSIVE PALLIDAL DEGENERATIONArchives of Neurology & Psychiatry, 1932