Two Siblings of Hyperphenylalaninemia: Suggestion to a Genetic Variant of Phenylketonuria
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A sibling case of hyperphenylalaninemia without phenylpyruvic aciduria was described. An oral loading of phenylalanine revealed a delay of clearance of serum phenylalanine, a slight elevation of serum tyrosine, and an increased urinary excretion of phenylpyTuvic acid and o-hydroxyphenylacetic acid. Phenylalanine hydroxylase in the liver was found to be of about one-tenth the normal activity. These findings suggest that hyperphenlyalaninemia may be a genetic variant of phenylketonuria.
- 東北ジャーナル刊行会の論文
東北ジャーナル刊行会 | 論文
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