In:
Neuropathology, Wiley, Vol. 34, No. 3 ( 2014-06), p. 309-313
Abstract:
Multiple system atrophy ( MSA ) is an oligodendrogliopathy of presumably sporadic origin, characterized by prominent α‐synuclein inclusions with neuronal multisystem degeneration, although a few M endelian pedigrees have been reported. Here we report two familial cases of MSA of unknown genetic background. One patient was diagnosed as a possible MSA ‐ C (cerebellar dysfuntion) case, and the other as clinically possible MSA ‐ P (parkinsonism), which turned out to be definite MSA , based on a detailed autopsy. The neuropathology showed extensive deposition of α‐synuclein in the glia as well as in the neurons located in the cerebral cortices and hippocampal systems, although neither multiplication of the SNCA gene or mutations in COQ2 gene were identified in the family concerned.
Type of Medium:
Online Resource
ISSN:
0919-6544
,
1440-1789
DOI:
10.1111/neup.2014.34.issue-3
Language:
English
Publisher:
Wiley
Publication Date:
2014
detail.hit.zdb_id:
2008290-3
Permalink