A new variant of late-onset myophosphorylase deficiency
โ Scribed by Gerald J. Kost; Dr. M. Anthony Verity
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 829 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract Two brothers presented in their midโforties with movement disorders including atypical parkinsonism, choreiform movements, stereotypies, ataxia and dysarthria. Both brothers showed putaminal lucencies on imaging and, in the proband, a deficiency of the pyruvate dehydrogenase complex (PD
The case of a 77-year-old woman ยฎrst diagnosed with kleptomania is presented to indicate a possible late-onset course of this disorder. Particularly striking about this patient's history of shoplifting behaviors was the absence of an onset prior to the age of 73. Her pattern of stealing did not begi
A family with hereditary amyloidosis characterized by peripheral neuropathy and cardiomyopathy is described. Lack of eye involvement sets their disease apart from the Indiana/Swiss familial amyloidotic polyneuropathy type 11. The disease is of late onset; affected members die of cardiomyopathy after