Hyperammonemia

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Hyperammonemia
File:Ammonia lone electron pair.svg
Ammonia molecule
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Confusion, lethargy, vomiting, seizures, coma
Complications Cerebral edema, brain damage
Onset Can be acute or chronic
Duration Varies depending on cause
Types N/A
Causes Liver disease, urea cycle disorders, medications, infections
Risks Genetic predisposition, liver failure, renal failure
Diagnosis Blood ammonia level, liver function tests, genetic testing
Differential diagnosis Hepatic encephalopathy, urea cycle disorder, metabolic disorders
Prevention N/A
Treatment Lactulose, antibiotics, dialysis, liver transplant
Medication Lactulose, Rifaximin, Sodium phenylbutyrate
Prognosis Depends on underlying cause and treatment
Frequency Rare
Deaths N/A


Hyperammonemia is a metabolic disturbance characterized by an excess of ammonia in the blood. It is a dangerous condition that can lead to brain damage and/or death. It may be primary or secondary. Ammonia is a substance that contains nitrogen. It is a byproduct of the breakdown of protein. It can be caused by genetic disorders, liver disease, or certain medications.

Causes[edit]

Hyperammonemia can be caused by a variety of factors, including:

Symptoms[edit]

Symptoms of hyperammonemia can vary depending on the severity of the condition. They may include:

Diagnosis[edit]

Hyperammonemia is diagnosed through a blood test that measures the level of ammonia in the blood. Additional tests may be needed to determine the underlying cause of the condition.

Treatment[edit]

Treatment for hyperammonemia typically involves addressing the underlying cause of the condition. This may include:

  • Medication: Drugs that reduce the amount of ammonia in the body, such as lactulose and rifaximin, may be used.
  • Dietary changes: A diet low in protein may be recommended to reduce the amount of ammonia produced by the body.
  • Dialysis: In severe cases, dialysis may be needed to remove excess ammonia from the blood.

See also[edit]