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Silent latency periods in methylmercury poisoning and in neurodegenerative disease.

This article discusses three examples of delay (latency) in the appearance of signs and symptoms of poisoning after exposure to methylmercury. First, a case is presented of a 150-day delay period before the clinical manifestations of brain damage after a single brief (<1 day) exposure to dimethyl...

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Detalles Bibliográficos
Autores principales: Weiss, Bernard, Clarkson, Thomas W, Simon, William
Formato: Texto
Lenguaje:English
Publicado: 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241259/
https://www.ncbi.nlm.nih.gov/pubmed/12426145
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author Weiss, Bernard
Clarkson, Thomas W
Simon, William
author_facet Weiss, Bernard
Clarkson, Thomas W
Simon, William
author_sort Weiss, Bernard
collection PubMed
description This article discusses three examples of delay (latency) in the appearance of signs and symptoms of poisoning after exposure to methylmercury. First, a case is presented of a 150-day delay period before the clinical manifestations of brain damage after a single brief (<1 day) exposure to dimethylmercury. The second example is taken from the Iraq outbreak of methylmercury poisoning in which the victims consumed contaminated bread for several weeks without any ill effects. Indeed, signs of poisoning did not appear until weeks or months after exposure stopped. The last example is drawn from observations on nonhuman primates and from the sequelae of the Minamata, Japan, outbreak in which low chronic doses of methylmercury may not have produced observable behavioral effects for periods of time measured in years. The mechanisms of these latency periods are discussed for both acute and chronic exposures. Parallels are drawn with other diseases that affect the central nervous system, such as Parkinson disease and post-polio syndrome, that also reflect the delayed appearance of central nervous system damage.
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spelling pubmed-12412592005-11-08 Silent latency periods in methylmercury poisoning and in neurodegenerative disease. Weiss, Bernard Clarkson, Thomas W Simon, William Environ Health Perspect Research Article This article discusses three examples of delay (latency) in the appearance of signs and symptoms of poisoning after exposure to methylmercury. First, a case is presented of a 150-day delay period before the clinical manifestations of brain damage after a single brief (<1 day) exposure to dimethylmercury. The second example is taken from the Iraq outbreak of methylmercury poisoning in which the victims consumed contaminated bread for several weeks without any ill effects. Indeed, signs of poisoning did not appear until weeks or months after exposure stopped. The last example is drawn from observations on nonhuman primates and from the sequelae of the Minamata, Japan, outbreak in which low chronic doses of methylmercury may not have produced observable behavioral effects for periods of time measured in years. The mechanisms of these latency periods are discussed for both acute and chronic exposures. Parallels are drawn with other diseases that affect the central nervous system, such as Parkinson disease and post-polio syndrome, that also reflect the delayed appearance of central nervous system damage. 2002-10 /pmc/articles/PMC1241259/ /pubmed/12426145 Text en
spellingShingle Research Article
Weiss, Bernard
Clarkson, Thomas W
Simon, William
Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title_full Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title_fullStr Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title_full_unstemmed Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title_short Silent latency periods in methylmercury poisoning and in neurodegenerative disease.
title_sort silent latency periods in methylmercury poisoning and in neurodegenerative disease.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241259/
https://www.ncbi.nlm.nih.gov/pubmed/12426145
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