Hyperammonemia Familial

Familial hyperammonemia is a rare genetic disorder that causes high levels of ammonia in the blood. It can be caused by a variety of reasons, including genetic mutations, liver and kidney problems, and certain medications.

Symptoms of familial hyperammonemia may include headache, weakness, nausea, vomiting, seizures, and loss of consciousness. In severe cases, brain damage and even death can occur.

Diagnosis of familial hyperammonemia includes a blood test for ammonia levels. Additional tests, such as ultrasound of the liver and kidneys, may also be prescribed.

Treatment for familial hyperammonemia depends on the cause of the disease. In some cases, hospitalization and intensive care may be required. In other cases, changing your diet and taking medications is enough.

Prevention of familial hyperammonemia involves following a diet, avoiding certain medications, and regular examination by a doctor.

Familial hyperammonemia can be prevented by following a diet, avoiding medications, and getting checked regularly by a doctor. If symptoms of hyperammonemia occur, you should immediately consult a doctor for diagnosis and treatment.

Familial hyperammonemia is called hyperammonemia, which, in addition to blood, is found in the cerebrospinal fluid, other brain tissues or organs of the excretory system, i.e. where there is a sufficient level of ammonia. It is believed that **familial hyperamminemia** **manifests either in connection with malignant brain tumors, or when “unfavorable genes” cause brain destruction.**

*Hyperammonia* is detected in malignant