Hereditary Tyrosinemia type I (HT-1) is a rare genetic disorder where the enzyme FAH is deficient, causing the accumulation of tyrosine and its byproducts in the liver, kidneys, and central nervous system. This can lead to severe liver disease due to the improper breakdown of tyrosine. Read the infographics below to learn about Tyrosinemia type 1 symptoms, diagnosis, treatment, management, challenges, research, etc.
Hereditary Tyrosinemia type I (HT-1) – Understanding a Rare Genetic Disorder
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