Methylmercury Poisoning in Canadian Indians — The Elusive Diagnosis

• Published in: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
• Main Authors: Wheatley, Brian, Barbeau, André, Clarkson, Thomas W., Lapham, Lowell W.
• Format: Article in Journal/Newspaper
• Language: English
• Published: Cambridge University Press (CUP) 1979
• Subjects: Canada; Indian; inuit
• Online Access: http://dx.doi.org/10.1017/s0317167100023817; https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0317167100023817

SUMMARY: A World Health Organization Expert Committee has concluded that symptoms of methylmercury poisoning may appear at blood concentrations of 200-500 ng Hg/ml. Blood levels in this range have been found in several Indian and Inuit communities in Canada. The syndrome of severe methylmercury poisoning (Hunter-Russell syndrome) is well described. However, diagnosis of less severe cases is difficult. This paper reviews the present situation in Canada. The problems of diagnosis currently being encountered are discussed and are illustrated by the case of an individual who had one of the highest blood concentrations (551 ng Hg/ml) ever described in fish-eating populations outside of the outbreaks in Minamata and Niigata in Japan. Although mercury concentrations in brain were estimated to have been in the “symptomatic” range at least once in the two years prior to his death, neurohisiological examination was normal. Detailed examination by two teams of neurologists revealed effects that may be associated with methylmercury poisoning but a definitive diagnosis remained elusive.