To investigate the interrelation of heavy metals and the influence on next generation, total mercury and methylmercury, lead, cadmium, manganese, copper, zinc, and iron were determined in the maternal blood, placenta, umbilical cord, and umbilical cord blood. Samples were collected at delivery from 231 pregnant women who were living in the city of Nagoya, located in the central district of Japan, during 1974 and 1978. Total mercury and methylmercury, cadmium, and iron were higher in cord blood than in maternal blood, whereas copper and zinc were lower. Significant positive correlations were observed between maternal and cord blood with regard to total mercury and methylmercury, lead, cadmium, and manganese contents. Significant correlations were also observed between many pairs of metals, particularly in umbilical cord and its blood.

We investigated the incidence of each pattern of the communications between the musculocutaneous and median nerves and discussed its morphological significance. The communications between both nerves were seen in 188 (41.5%) of 453 specimens. They were classified into five regular patterns according to their directions and formations. The incidence of the communication was significantly higher in those with excessive heads of biceps brachii than in those without them (p < 0.05). As a result, we established a classification of the regular pattern of the communications and revealed that the musculocutaneous and median nerves had the possibility of forming plexuses in the humeral area. The musculocutaneous nerves are regarded as the bundles that arise from the median nerve with the lateral cutaneous nerve of forearm and the branches to the biceps brachii and brachialis muscles.

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To evaluate the prevalence of dihydropyrimidinuria (DHPuria), we analyzed urine samples from 21,200 healthy Japanese infants, and found two cases of DHPuria without clinical symptoms. Based on this result, we estimated the prevalence to be approximately 1/10,000 births in Japan. In addition, we analyzed pyrimidine catabolism on a previously reported family with an adult DHPuria case. We newly identified the sister of the propositus as the second case of DHPuria in this family, because she excreted large amounts of dihydrouracil and dihydrothymine. The parents and the child of the propositus showed slight increases of dihydrouracil and dihydrothymine. This is the first family with 2 cases of DHPuria, indicating that DHPuria is an inherited condition. To determine the inheritance of DHPuria in this family and to examine the risk of 5-fluorouracil (5-FU) toxicity, a uracil loading test was performed on the parents. Urinary dihydrouracil concentrations in the parents after the loading were several times higher than those in normal control persons, the finding being consistent with DHPuria heterozygotes. This, along with data on the propositus, his sister, and his child, indicates that DHPuria is an autosomal recessive condition. In addition, DHPuria homozygotes may have a high risk of 5-FU toxicity, while the risk is relatively low in heterozygotes.