| Literature DB >> 7276985 |
A Staal, S Z Stefanko, H F Busch, F G Jennekens, W C De Bruinj.
Abstract
This report concerns an unusual form of olivopontocerebellar atrophy (OPCA) of adult onset, inherited as an autosomal dominant. We examined 5 patients in one generation and performed neuropathological investigations in 3 of these. The clinical and pathological features were different from those of OPCA types I to V. Apart from olivopontocerebellar degeneration, there was dementia in 4, massive atrophy of the spinal cord in 3, and focal degeneration of the optic nerves in at least 1 case. The most remarkable findings were, however, the involvement of the peripheral nervous system and the abundant intrafascicular calcification in sympathetic nerve fibers and in their ganglia.Entities:
Mesh:
Year: 1981 PMID: 7276985 DOI: 10.1016/0022-510x(81)90116-7
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181