genetic
Tyrosinemia
Tyrosinemia or tyrosinaemia is an error of , usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms of untreated tyrosinemia include liver and kidney disturbances. Without treatment, tyrosinemia leads to liver failure. Today, tyrosinemia is increasingly detected on newborn tests before any symptoms appear. With early and lifelong management involving a low- diet, special protein formula, and sometimes medication, people with tyrosinemia develop normally, are healthy, and live normal lives.
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