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.

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Centro Editorial Universidad de Caldas. This page was last edited on 30 Septemberat An essential nutrient for the cat. Overstimulation of NMDA-receptors induces excitotoxicity. Services on Demand Article. Hiperamonemoa solamente apoproteina B Infobox medical condition new. J Am Vet Med Assoc.

A brief review of the biochemistry of its requirement and the clinical consequences of deficiency.

Fundamentos bioquímicos de la Hiperamonemia tipo I by brenda paola hernandez soto on Prezi

Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Treatment centers on limiting intake of ammonia and increasing its excretion.


Phenylbutyratewhich is the product of phenylacetate, conjugates with glutamine to form phenylacetylglutaminewhich is excreted by the kidneys. Retrieved from ” https: Views Read Edit View history.

Hyperammonemia – Wikipedia

Niperamonemia is a substance that contains nitrogen. Amino acid metabolism disorders. The present review analyses and updates the reader about domestic feline metabolism, through the following sections: J Feline Med Surg.

Inborn error of amino acid metabolism E70—E72 It may be primary or secondary. Intravenous arginine argininosuccinase deficiency sodium phenylbutyrate and sodium benzoate ornithine transcarbamoylase deficiency are pharmacologic agents commonly used as adjunctive therapy to treat hyperammonemia in patients with urea cycle enzyme deficiencies.

Cystinuria Hartnup disease Iminoglycinuria Lysinuric protein intolerance Fanconi syndrome: Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria. 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. Dietary protein, a metabolic source of ammonium, is restricted and caloric intake is provided by glucose and fat. Dopamine beta hydroxylase deficiency reverse: Contienen las apoproteinas BE y C.

Expert Consult – Online and Print. Histidine Carnosinemia Histidinemia Urocanic aciduria. Limusa Grupo Noriega Editores.


Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia. It is a dangerous condition that may lead to brain injury and death.

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. Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease.

GAMT deficiency Glycine encephalopathy. This is a treatment for hepatic encephalopathy.


Obtenido en agosto dedesde http: Se requieren cofactores, como: By using this site, you agree to the Terms of Use and Privacy Policy. Obtenido en noviembre dedesde http: It is a product of the catabolism of protein. Abstract The present review analyses and updates the reader about domestic feline metabolism, through the following sections: How to cite this article. In other projects Wikimedia Commons.

Ocular albinism 1 Oculocutaneous albinism Hermansky—Pudlak syndrome Waardenburg syndrome. El acetil-CoA y el malonil-CoA, se condensan formando acetil-malonil. D ICD –