Tyrosinaemia Type 1 is a rare life-threatening genetic disorder present from birth. In Tyrosinaemia Type 1, the body is unable to break down an amino acid called tyrosine. This causes a build up of tyrosine and another chemical called succinylacetone in the liver, kidneys, eyes and brain and can cause problems. At present, the treatment … Continue reading Tyrosinaemia Type 1