Hyperammonemia (or hyperammonaemia) is a metabolic disturbance characterised by an Hyperammonemia is one of the metabolic derangements that contribute to hepatic encephalopathy, which can cause swelling of astrocytes and. 31 jul. Doenças de depósito lisossômico (2 mucopolissacaridoses tipo 1; 1 suspeitos e confirmados de EIM, foi a hiperamonemia, seguida pela. Na tirosinemia hereditária ou tipo 1, além do tratamento dietético com Acidúria glutárica tipo 1 .. A hiperamonemia representa uma urgência metabólica.

Author: Zologami Tesida
Country: Belgium
Language: English (Spanish)
Genre: Personal Growth
Published (Last): 10 January 2005
Pages: 467
PDF File Size: 15.42 Mb
ePub File Size: 6.1 Mb
ISBN: 910-9-75002-296-6
Downloads: 26478
Price: Free* [*Free Regsitration Required]
Uploader: Kegal

By using this site, you agree to the Terms of Use and Privacy Policy.

The metabolic pathways that synthesize urea involve reactions that start in the mitochondria and then move into the cytosol. Carnosinemia Histidinemia Urocanic aciduria.

Obtenido en agosto dedesde http: Ammonia is a substance that contains nitrogen. Contienen solamente apoproteina B Services on Demand Article. Dopamine beta hydroxylase deficiency reverse: Amino acid metabolism disorders. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. How to cite this article. It is a product of the catabolism of protein.


This page was last edited on 30 Septemberat Se requieren cofactores, como: The present review analyses and updates the reader about domestic feline metabolism, through the following sections: Retrieved from ” https: El acetil-CoA y el malonil-CoA, se condensan formando acetil-malonil.

Ocular albinism 1 Oculocutaneous albinism Hermansky—Pudlak syndrome Waardenburg syndrome.

It is a dangerous condition that may lead to brain injury and death. This is a treatment for hepatic encephalopathy. GAMT deficiency Glycine encephalopathy. Phenylbutyratewhich is the product of phenylacetate, conjugates with glutamine to form phenylacetylglutaminewhich is excreted by the kidneys. Similarly, sodium benzoate reduces ammonia content in the blood by conjugating with glycine to form hippuric acidwhich is rapidly excreted by the kidneys.

Su deficiencia, se debe a la incapacidad del organismo de sintetizar la ornitina, un precursor de la arginina CASE et al. From Wikipedia, the free encyclopedia. Views Read Edit View history. It is converted to the less toxic substance urea prior to excretion in urine by the kidneys.

Infobox medical condition new. Hipetamonemia error of amino acid metabolism E70—E72 Dietary protein, a metabolic source of ammonium, is restricted and caloric intake is provided by glucose and fat.



Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria. J Feline Med Surg. In other projects Wikimedia Commons. Centro Editorial Universidad de Caldas. Overstimulation of NMDA-receptors induces excitotoxicity. A brief review of the biochemistry of its requirement and the clinical consequences of deficiency.


Limusa Grupo Noriega Editores. Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia. It may be primary or secondary.

D ICD – Treatment centers on limiting intake of ammonia and increasing its excretion. An essential nutrient for the cat. Hyperammonemia or hyperammonaemia is a metabolic disturbance characterised by an excess of ammonia in the blood.

Hyperammonemia is one of the metabolic derangements that contribute to hepatic encephalopathywhich can cause swelling of astrocytes and stimulation of NMDA-receptors in the brain. Obtenido en noviembre dedesde http: Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease.

This article was written by admin