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4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
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. Additional recommended knowledge
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| This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "4-Alpha-hydroxyphenylpyruvate_hydroxylase_deficiency". A list of authors is available in Wikipedia. |
