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MERCURY 305<br />

2. HEALTH EFFECTS<br />

<strong>for</strong> psychological development) (Thorpe et al. 1992). Mercury exposure was not measured, but the child was<br />

born with hair levels of 3 mg/kg (3 ppm) of mercury. This hair level was comparable to that observed in<br />

populations consuming fish once a week (WHO 1990) <strong>and</strong> suggests that exposure in this case may have been<br />

relatively low.<br />

In the in vivo study by Sager et al. (1982), it was concluded that methylmercury may be acting on mitotic<br />

spindle microtubules leading to cell injury in the developing cerebellar cortex. Cell injury observed in the<br />

external granular layer of the cerebellar cortex of 2-day-old rats was attributed to a reduced percentage of<br />

late mitotic figures (arrested cell division) due to the loss of spindle microtubules. Mitosis <strong>and</strong> migration of<br />

granule cells in the cerebellum end within weeks following birth; there<strong>for</strong>e, this observation may suggest<br />

potential differences in the sensitivities of children <strong>and</strong> adults to mercury-induced neurotoxicity.<br />

Regardless of whether mercury exposure is through inhalation of mercury vapors, ingestion of organic<br />

mercury or mercury salts, or dermal application of mercury-containing ointments, patients (primarily<br />

children) may exhibit a syndrome known as acrodynia, or pink disease. Acrodynia is often characterized by<br />

severe leg cramps; irritability; <strong>and</strong> erythema <strong>and</strong> subsequent peeling of the h<strong>and</strong>s, nose, <strong>and</strong> soles of the feet.<br />

Itching, swelling, fever, tachycardia, elevated blood pressure, excessive salivation or perspiration,<br />

morbilli<strong>for</strong>m rashes, fretfulness, sleeplessness, <strong>and</strong>/or weakness may also be present. It was <strong>for</strong>merly<br />

thought that this syndrome occurred exclusively in children, but recent reported cases in teenagers <strong>and</strong> adults<br />

have shown that these groups are also susceptible.<br />

Developmental effects from prenatal or postnatal exposures to mercury are unique to children. During<br />

critical periods of structural <strong>and</strong> functional development in both prenatal <strong>and</strong> postnatal life, children are<br />

especially vulnerable to the toxic effects of mercury. Inhalation exposures are relatively rare outside of the<br />

occupational setting so the exposure route <strong>and</strong> <strong>for</strong>m of mercury most commonly associated with a risk <strong>for</strong><br />

development effects is the ingestion of methylmercury on the surface of contaminated foods (methylmercury<br />

used as a fungicide on seed grain) or accumulated within the food (methylmercury in fish, wild game, <strong>and</strong><br />

marine mammals). The exposure route <strong>and</strong> <strong>for</strong>m of mercury most commonly associated with maternal<br />

exposures is to foods contaminated with methylmercury fungicides (Bakir et al. 1973) or foods that contain<br />

high levels of methylmercury (Gr<strong>and</strong>jean et al. 1997b, 1998; Tsubaki <strong>and</strong> Takahashi 1986).<br />

The first such incident was reported in Sweden in 1952 when flour from grain treated with an unspecified<br />

alkyl mercury compound ingested by a pregnant woman was associated with developmental toxicity. An

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