Aminoacidemia

Aminoacidemias are a group of inherited disorders of amino acid metabolism that impair the normal functioning of the body, including the brain, muscles and other organs. These diseases occur due to a deficiency of enzymes that are involved in the metabolism of amino acids.

Aminoacidemia can be caused by a variety of causes, including genetic mutations, liver or kidney disease, and medications that can inhibit enzymes involved in metabolism. Symptoms of aminoacidemias may include fatigue, loss of appetite, nausea, vomiting, muscle weakness and loss of consciousness.

Treatment of aminoacidemia may include treatment of the underlying disease that led to disruption of amino acid metabolism. In some cases, intravenous amino acids may be required to maintain normal amino acid levels in the body.

In general, aminoacidaemias are serious diseases that require early diagnosis and treatment. Timely intervention can help prevent the development of complications and improve the quality of life of patients.

Aminoacidemia

Aminoacidemia or hyperaminacidemia is a pathology of the metabolism of amino acids - a group of organic compounds. Along the way, amino acids are not completely broken down. This process leads to the formation of under-oxidized products that are toxic to the body. In conditions of excess of such substrates, toxins enter the blood. The presence of such processes in the body leads to the fact that a person feels worse - he develops weakness, malaise, and decreases activity.