Hyperammonemia
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Ammonia | |
ICD-10 | E72.2 |
ICD-9 | 270.6 |
DiseasesDB | 20468 |
eMedicine | neuro/162 ped/1057 |
MeSH | D022124 |
Hyperammonemia (or 'hyperammonaemia') is a metabolic disturbance characterised by an excess of ammonia in the blood. It is a dangerous condition that may lead to encephalopathy and death. It may be primary or secondary.
Ammonia is a substance that contains nitrogen. It is a product of the catabolism of protein. It is converted to the non-toxic substance urea prior to excretion in urine by the kidneys. The metabolic pathways that synthesise urea are located first in the mitochondria and then into the cytosol. The process is known as the urea cycle, which comprises several enzymes acting in sequence.
Contents |
[edit] Types
[edit] Primary vs. secondary
- Primary hyperammonemia is caused by several inborn errors of metabolism that are characterised by reduced activity of any of the enzymes in the urea cycle.
- Secondary hyperammonemia is caused by inborn errors of intermediary metabolism characterised by reduced activity in enzymes that are not part of the urea cycle (e.g .Propionic acidemia, Methylmalonic acidemia) or dysfunction of cells that make major contributions to metabolism (eg hepatic failure).
[edit] Specific types
In all cases Hyperammonemia results from defects of the Urea cycle. The following list includes such examples:
- Mendelian Inheritance in Man (OMIM) 311250 - hyperammonemia due to ornithine transcarbamylase deficiency
- Mendelian Inheritance in Man (OMIM) 606762 - hyperinsulinism-hyperammonemia syndrome
- Mendelian Inheritance in Man (OMIM) 238970 - hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- Mendelian Inheritance in Man (OMIM) 237310 - hyperammonemia due to N-acetylglutamate synthetase deficiency
- Mendelian Inheritance in Man (OMIM) 237300 - hyperammonemia due to carbamoyl phosphate synthetase i deficiency
- Mendelian Inheritance in Man (OMIM) 238750 - hyperlysinuria with hyperammonemia
[edit] Sequelae
Hyperammonemia is one of the metabolic derangements that contribute to the encephalopathy associated with hepatic failure.