Some articles on type iii tyrosinemia:
... Type III tyrosinemia is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 126.96.36.199), encoded by the gene HPD ... Characteristic features of type III tyrosinemia include mild mental retardation, seizures, and periodic loss of balance and coordination (intermittent ataxia) ... Type III tyrosinemia is very rare only a few cases have been reported ...
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