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ICD-10 code: E70.5

Disease category: E70.5: Disorders of tryptophan metabolism

Disorders of Tryptophan Metabolism

Tryptophan is an essential amino acid that plays a crucial role in several physiological processes in the human body. It is obtained through dietary sources and is converted into various compounds necessary for the proper functioning of the body. However, certain disorders can affect the metabolism of tryptophan, leading to potential health issues.

Here are some common disorders associated with tryptophan metabolism:

  1. Kynureninuria: This disorder is characterized by the excessive excretion of kynurenine, a metabolite of tryptophan, in urine. It is caused by a deficiency of enzymes involved in the kynurenine pathway. Kynureninuria can lead to neurological symptoms such as intellectual disability, seizures, and behavioral abnormalities.
  2. Hartnup disease: It is an autosomal recessive disorder that affects the absorption of tryptophan and other neutral amino acids in the intestine and kidney. This results in low levels of tryptophan in the body, leading to various symptoms including photosensitivity, skin rashes, and neurological problems.
  3. Hypertryptophanemia: In this disorder, there is an elevated level of tryptophan in the blood. It is caused by the deficiency of enzymes involved in the metabolism of tryptophan. Hypertryptophanemia can lead to neurological symptoms, such as cognitive impairment and developmental delay.
  4. Serotonin syndrome: Although not directly related to tryptophan metabolism disorders, serotonin syndrome can occur due to the excessive production or accumulation of serotonin. Tryptophan is a precursor for serotonin synthesis. Serotonin syndrome can result from the use of certain medications or drug interactions, leading to symptoms such as agitation, confusion, and rapid heart rate.

These disorders of tryptophan metabolism can significantly impact an individual's health and well-being. Early diagnosis and appropriate management are essential to mitigate the symptoms and improve the quality of life for those affected. If you suspect any of these disorders, it is important to consult with a healthcare professional for proper evaluation and guidance.

While treatment options are available for these disorders, it is beyond the scope of this article to discuss them in detail. Nevertheless, understanding the existence of these disorders and their potential impacts can help raise awareness and promote further research in the field of tryptophan metabolism.

Treatment of Disorders of tryptophan metabolism:

Treatment Options for Disorders of Tryptophan Metabolism

Disorders of tryptophan metabolism are a group of rare genetic conditions that affect the body's ability to properly process tryptophan, an essential amino acid. These disorders can lead to a range of symptoms and complications, making early diagnosis and appropriate treatment essential. Here are some treatment options for in...

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