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Traducción y análisis de palabras por inteligencia artificial ChatGPT
En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:
- cómo se usa la palabra
- frecuencia de uso
- se utiliza con más frecuencia en el habla oral o escrita
- opciones de traducción
- ejemplos de uso (varias frases con traducción)
- etimología
Qué (quién) es ketotic hyperglycinemia - definición
ORGANIC ACIDEMIA THAT INVOLES A NONFUNCTIONAL PROPIONYL COA CARBOXYLASE AFFECTING CONVERSION OF AMINIO ACIDS AND FATS INTO SUGAR FOR ENERGY
Acidemia, propionic; Ketotic glycinemia; Propionic aciduria; Propionyl-CoA carboxylase deficiency
Glycine encephalopathy
AMINO ACID METABOLIC DISORDER THAT INVOLVES ABNORMALLY HIGH LEVELS OF THE AMINO ACID GLYCINE IN BODILY FLUIDS AND TISSUES
Nonketotic hyperglycinemia; Hyperglycinemia, nonketotic; NKH; Non-ketotic hyperglycinemia; Glycine Encephalopathy (Nonketotic Hyperglycinemia); Non-ketotic hyperglycinaemia
Glycine encephalopathy is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism.
Propionic acidemia
Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase deficiency (PCC deficiency), is a rare autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia.
Hyperglycinemia
WIKIMEDIA DISAMBIGUATION PAGE
Hyperglycinemia (disambiguation)
Hyperglycinemia may refer to one of two related inborn amino acid disorders that are characterized by elevated levels of glycine in the blood.
Wikipedia
Propionic acidemia
Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase deficiency (PCC deficiency), is a rare autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia.
The disorder presents in the early neonatal period with poor feeding, vomiting, lethargy, and lack of muscle tone. Without treatment, death can occur quickly, due to secondary hyperammonemia, infection, cardiomyopathy, or brain damage.
