Type 1 Tyrosinemia, also known as hepatorenal tyrosinemia, is the most severe form of tyrosinemia. It is caused by a deficiency of the enzyme fumarylacetoacetate hydrolase and p-hydroxyphenylpyruvic acid oxidase.
Drugs used to treat Hereditary Tyrosinemia Type 1
| Name | Drug Class |
|---|---|
| Nitisinone | Miscellaneous metabolic agents |
| Orfadin | Miscellaneous metabolic agents |
| Nityr | Miscellaneous metabolic agents |
