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HERO ID
2305170
Reference Type
Journal Article
Subtype
Review
Title
Minamata disease
Author(s)
Eto, K
Year
2000
Is Peer Reviewed?
1
Journal
Neuropathology
ISSN:
0919-6544
EISSN:
1440-1789
Volume
20
Page Numbers
S14-S19
Language
English
PMID
11037181
Web of Science Id
WOS:000165409400005
Abstract
Minamata disease (methylmercury poisoning) was first discovered in 1956 around Minamata Bay, Kumamoto Prefecture, Japan. A second epidemic in Japan occurred in 1965 along the Agano River, Niigata Prefecture. This paper presents a brief review of Minamata disease with an emphasis on the cases found in Kumamoto Prefecture. At autopsy, the most conspicuous destructive lesion in the cerebrum was found in the anterior portions of the calcarine cortex. Less severe but similar lesions may be found in the post-central, pre-central and temporal transverse cortices. Secondary degeneration from primary lesions may be seen in cases with long survival. In the cerebellum, pathological changes occur deep in the hemisphere. The granule cell population was more affected, compared with Purkinje cells. Among peripheral nerves, sensory nerves were more affected than motor nerves. Our recent experimental studies that reveal knowledge of the pathogenesis of methylmercury poisoning will be discussed.
Keywords
human autopsy cases; methylmercury poisoning; pathogenesis
Tags
IRIS
•
Methylmercury
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