Aminoaciduria Overload

Aminoaciduria is a group of hereditary diseases associated with impaired amino acid metabolism in the body. In this article we will look at overload aminoaciduria (syn. A. prerenal).

Aminoaciduria is a genetic disease that is associated with impaired synthesis or breakdown of amino acids in the liver, kidneys or intestines. With this disease, the level of certain amino acids in the blood increases, which leads to disruption of the functions of organs and body systems.

The main symptom of aminoaciduria is vomiting, which can be caused by impaired absorption of amino acids in the intestine. Disturbances in the functioning of the kidneys, liver and nervous system may also occur.

Treatment of overload aminoaciduria consists of correcting amino acid metabolism and maintaining the functions of organs and systems. Depending on the type of amino acid that is causing the disease, different medications may be used.

For example, if you have a tryptophan deficiency, you may need to take medications containing tryptophan, and if you have a lysine deficiency, you may need to take medications that contain lysine. You may also need to prescribe medications to support liver and kidney function.

In addition, it is important to ensure proper nutrition, which will contain sufficient amounts of essential amino acids.

In general, overload aminoaciduria is a serious disease that requires timely diagnosis and treatment.

**Aminoacidopathy** is a group of hereditary disorders of amino acid metabolism that lead to their accumulation in biological fluids and tissues. Diseases are rare, more than 250 different forms have been described, and among them there are diseases associated with the accumulation of free histidine or the citrulline fraction