• Tyrosinemia - Genetics Home Reference

    ghr.nlm.nih.gov/condition/tyrosinemia Tyrosinemia is a genetic disorder characterized by disruptions in the multistep process that breaks down the amino acid tyrosine, a building block of most ...
  • Tyrosinemia: Background, Pathophysiology, Epidemiology

    emedicine.medscape.com/article/949816-overview Hereditary infantile tyrosinemia, or tyrosinemia I, is a completely different disease. Patients have a peculiar (cabbagelike) odor, renal tubular ...
  • Tyrosinemia - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Tyrosinemia There are three types of tyrosinemia, each with distinctive symptoms and caused by the deficiency of a different enzyme. Type I tyrosinemia; Type II tyrosinemia
    • Tyrosinemia Symptoms & Treatment | Children's Hospital Pittsburgh

      www.chp.edu/our-services/transplant/liver/education/.../tyrosinemia Learn about Tyrosinemia, a disorder where the body lacks an enzyme to metabolize tyrosine. Discover the symptoms and treatment.
    • Tyrosinemia Symptoms, Diagnosis, Treatments and Causes ...

      www.rightdiagnosis.com/t/tyrosinemia/intro.htm Tyrosinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
    • Tyrosinemia - NEWBORN SCREENING

      www.newbornscreening.info/Parents/aminoaciddisorders/Tyrosinemia.html What causes tyrosinemia 1? In order for the body to use protein from the food we eat, it is broken down into smaller parts called amino acids. Special enzymes then ...
    • Tyrosinemia Type I - GeneReviews┬« - NCBI Bookshelf

      www.ncbi.nlm.nih.gov/books/NBK1515 Untreated tyrosinemia type I usually presents either in young infants with severe liver involvement or later in the first year with liver dysfunction and renal ...
    • Newborn Screening Program - Tyrosinemia - IDPH

      www.idph.state.il.us/HealthWellness/fs/tyrosinemia.htm Tyrosinemia Information for Physicians and Other Health Care Providers Definition. The tyrosinemias are a group of inherited disorders of amino acid metabolism, each ...
    • Tyrosinemia - Causes of Tyrosinemia - Tyrosinemia ... - Liver

      www.liver.ca/liver-disease/types/tyrosinemia.aspx Tyrosinemia is caused by an absence of the enzyme fumarylacetoacetate hydrolase (FAH) which is essential in the metabolism of tyrosine.
    • Tyrosinemia Type 1 - WebMD

      www.webmd.com/children/tyrosinemia-hereditary Important It is possible that the main title of the report Tyrosinemia, Hereditary is not the name you expected. Please check the synonyms listing to find the ...