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En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:
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pyruvate carboxylase deficiency - traducción al árabe
HUMAN DISEASE
Pyruvate carboxylase deficiency disease; Ataxia with Lactic Acidosis, Type II; PC deficiency; Deficiency of pyruvate carboxylase
pyruvate carboxylase deficiency
عَوَزُ كَرْبُوكسيلازُ البَيرُوفات
pyruvate carboxylase
![[[Pyruvic acid]]](https://commons.wikimedia.org/wiki/Special:FilePath/Pyruvic-acid-2D-skeletal.png ?width=200 "[[Pyruvic acid]]")
![[[Oxaloacetic acid]]](https://commons.wikimedia.org/wiki/Special:FilePath/Oxaloacetic acid.png ?width=200 "[[Oxaloacetic acid]]")
MAMMALIAN PROTEIN FOUND IN HOMO SAPIENS
Pyruvate carboxyltransferase; Pyruvate carboxytransferase; EC 6.4.1.1; Pyruvate:carbon-dioxide ligase (ADP-forming)
كَرْبُوكسيلازُ البَيرُوفات
methylcrotonoyl-CoA carboxylase
CLASS OF ENZYMES
Methylcrotonoyl-CoA carboxylase; MCCC2; MCCC1; 3-methylcrotonyl-CoA carboxylase; EC 6.4.1.4; 3-methylcrotonoyl-CoA:carbon-dioxide ligase (ADP-forming); MC-CoA carboxylase
كَرْبوكْسِيلاز ميثيل كرُوتُونُوِيل التَميمِ A
Definición
Beriberi
·noun An acute disease occurring in India, characterized by multiple inflammatory changes in the nerves, producing great muscular debility, a painful rigidity of the limbs, and cachexy.
Wikipedia
Pyruvate carboxylase deficiency
Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. Type A of the disease appears to be much more common in some Algonkian Indian tribes in eastern Canada, while the type B disease is more present in European populations.
