4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

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4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency (also called Hawkinsinuria) is an autosomal dominant inborn error of metabolism. It is characterised by transient metabolic acidosis and tyrosinemia.

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is inherited in an autosomal dominant fashion.
4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is inherited in an autosomal dominant fashion.

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