Friday, January 25, 2019

Hyperammonemia : Signs, Symptoms And Treatment





Hyperammonemia

Hyperammonemia (or hyperammonaemia) is metabolic disturbance characterized by ammonia in the blood. This is a dangerous situation which can cause brain injury and death. It can be primary or secondary.
Ammonia is a substance in which nitrogen is present. This is a product of protein synthesis. Before immersion of urine in urine, it is converted into less poisonous substances urea. Metabolic pathways that synthesize urea include reactions that start in mitochondria and then go into cytosol. The procedure is known as urea cycle, in which many enzymes are employed in sequence.

Signs and Symptoms

Complication

Hyperammonemia is one of the metabolic inadequacies that contributes to hepatic encephalopathy, which can cause inflammation of the astrocytes in the brain and stimulation of NMDA-receptors. The susceptibility of NMDA-receptors leads to stimulation.

Diagnosis

Type

Primary vs. Secondary

•  Primary hyperammonemia is due to many innate errors in metabolism, which is characterized by the low activity of any activity of enzymes in the urea cycle. The most common example is ornithine transcarbamylase deficiency, which is inherited in X-linked fashion.
•  Secondary hyperammonemia is caused by the inborn errors of mediated metabolism, which is characterized by low activity of enzymes, which are not part of the urea cycle or failure of cells that make major contributions to metabolism. Examples of the former are propionic acidemia and  methylmalonic acidemia,, and later examples are hepatic cirrhosis with severe liver failure and hepatic failure.

Acquired vs. congenital

•  Acquired hyperammonemia is usually caused by diseases, which results in acute hepatic failure, such as exposure to overwhelming hepatitis B or hepatocytes, or cirrhosis of the liver, with older hepatic failure. Chronic hepatitis B, chronic hepatitis C, and excessive alcohol consumption are common causes of cirrhosis. Physical results of cirrhosis include the reduction of blood from the liver at least in vena cava, resulting in reduced blood filtration and removal of nitrogen-rich toxic substances by the liver and then hyperammonemia. In order to kill bacteria that initially produce ammonia, this kind of hyperammonemia can be treated with antibiotics, although this does not work, as well as to remove proteins from its digestion to ammonia, often lactulose administration Is achieved by (3-4 per day) bowel movement.
•  Drug induced hyperammonemia can occur with Valproic acid overdose, and due to lack of carnitine. Its treatment is the carnitine replacement.
•  Acute dehydration and bacterial overflow in small intestines can also cause hyperammonemia.
•  Glycine poisoning causes hyperammonemia, which appears in the form of symptoms and nausea of ​​CNS. Transient blindness can also occur.
•  Congenital hyperammonemia is usually caused by genetic defects in the urea cycle enzymes, such as ornithine transcarbamylase deficiency, which leads to low production of urea from ammonia. Read More


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