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Other disorders of tyrosine metabolism Save


ICD-10 code: E70.29

Disease category: E70.2: Disorders of tyrosine metabolism

Other Disorders of Tyrosine Metabolism: Symptoms and Causes

Tyrosine is an amino acid that plays a vital role in the human body. It is used to create neurotransmitters that regulate mood and cognitive functions, as well as hormones that control blood pressure and heart rate. However, when the body is unable to properly metabolize tyrosine, it can lead to a variety of disorders.

  1. Alkaptonuria:
  2. Alkaptonuria is a rare genetic disorder that affects the way the body processes tyrosine and phenylalanine. People with alkaptonuria have a deficiency of an enzyme called homogentisic acid oxidase, which causes a buildup of homogentisic acid in the body. This acid can cause arthritis, heart problems, and dark urine.

  3. Hereditary Tyrosinemia:
  4. Hereditary tyrosinemia is a genetic disorder that affects the liver's ability to process tyrosine. It is caused by a deficiency of the enzyme fumarylacetoacetate hydrolase, which leads to a buildup of toxic substances in the liver. Symptoms of hereditary tyrosinemia may include liver damage, kidney problems, and neurological symptoms.

  5. Phenylketonuria (PKU):
  6. Phenylketonuria (PKU) is a genetic disorder that affects the way the body processes phenylalanine, which is a component of tyrosine. People with PKU have a deficiency of the enzyme phenylalanine hydroxylase, which leads to a buildup of phenylalanine in the body. This can lead to intellectual disability, developmental delays, and seizures.

  7. Tyrosinemia:
  8. Tyrosinemia is a genetic disorder that affects the liver's ability to process tyrosine. It is caused by a deficiency of the enzyme fumarylacetoacetate hydrolase, which leads to a buildup of toxic substances in the liver. Symptoms of tyrosinemia may include liver damage, kidney problems, and neurological symptoms.

Other disorders of tyrosine metabolism may include oculocutaneous tyrosinemia, tyrosine hydroxylase deficiency, and dopa-responsive dystonia. The symptoms and causes of these disorders can vary widely, but they all involve a disruption in the body's ability to properly metabolize tyrosine.

In Conclusion

It is important to recognize the symptoms of tyrosine metabolism disorders and seek medical attention if you suspect that you or a loved one may be affected. While there is no cure for these disorders, early diagnosis and

Treatment of Other disorders of tyrosine metabolism:

Treatment Options for Other Disorders of Tyrosine Metabolism

Tyrosine is an amino acid that plays a crucial role in the body's metabolic processes. It is used to produce neurotransmitters, hormones, and other important compounds. However, some people are born with genetic mutations that affect their ability to metabolize tyrosine, leading to a range of disorders collectively known ...

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