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  2. Tyrosinemia type I - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_I

    Clinical treatment of HT1 relies on medications and strict ... doubts emerged that the underlying biochemical cause of hepatorenal tyrosinemia was a defective form of ...

  3. Tyrosinemia - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia

    Without treatment, tyrosinemia leads to liver failure. [1] Today, tyrosinemia is increasingly detected on newborn screening tests before any symptoms appear. With early and lifelong management involving a low-protein diet, special protein formula, and sometimes medication, people with tyrosinemia develop normally, are healthy, and live normal ...

  4. Nitisinone - Wikipedia

    en.wikipedia.org/wiki/Nitisinone

    [5] [6] This is a treatment for patients with Tyrosinemia type 1 as it prevents the formation of 4-Maleylacetoacetic acid and fumarylacetoacetic acid, which have the potential to be converted to succinyl acetone, a toxin that damages the liver and kidneys. [4] This causes the symptoms of Tyrosinemia type 1 experienced by untreated patients.

  5. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Medications E.g., Nitisinone prevents the formation of toxic metabolites for patients with Tyrosinemia Type I and enables normal growth and development in combination with a low-protein diet; Vitamins. E.g., thiamine supplementation benefits several types of disorders that cause lactic acidosis.

  6. Tyrosinemia type II - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_II

    Type II tyrosinemia is caused by a deficiency of the enzyme tyrosine aminotransferase (EC 2.6.1.5), encoded by the gene TAT.Tyrosine aminotransferase is the first in a series of five enzymes that converts tyrosine to smaller molecules, which are excreted by the kidneys or used in reactions that produce energy.

  7. What does growth hormone therapy treat? What an ... - AOL

    www.aol.com/does-growth-hormone-therapy-treat...

    What causes growth hormone deficiency? GHD is a relatively rare condition. Slowed growth, short stature, and low blood glucose levels in infants and toddlers are among a few signs of GH deficiency ...

  8. Tyrosinemia type III - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_III

    Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27), encoded by the gene HPD. [2] This enzyme is abundant in the liver, and smaller amounts are found in the kidneys. It is one of a series of enzymes needed to break down tyrosine.

  9. Dying To Be Free - The Huffington Post

    projects.huffingtonpost.com/dying-to-be-free...

    The medication, along with methadone treatment and needle exchange initiatives, also helped cut in half the HIV rate among intravenous drug users. By 2004, almost all of Australia’s heroin addicts in treatment were on methadone or buprenorphine, and the country had reduced its overdose deaths.