acidemia in English

noun

abnormal acidity of the blood (Medicine)

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Below are sample sentences containing the word "acidemia" from the English Dictionary. We can refer to these sentence patterns for sentences in case of finding sample sentences with the word "acidemia", or refer to the context using the word "acidemia" in the English Dictionary.

1. Metabolic Acidosis can lead to acidemia, which is defined as arterial blood pH that is lower than 7.35.

2. That failed Accelerations at stimulation tests are predictive of fetal acidemia 2, as stated by other authors and national guidelines 3

3. Other rare congenital defects are methylmalonic acidemia, a functional vitamin B12 deficiency, and biotin-responsive multiple carboxylase deficiency.

4. In any patient under total parenteral nutrition who develops an unexplained hyperlactic acidemia the possibility of thiamine deficiency should be suspected and treated.

5. Clinical manifestation. Clinical manifestations of the disease are hypoglycemia, lactic acidemia, hyperlipidemia, hyperuricemia, neutropenia and impaired neutrophil function, resulting in recurrent bacterial infections and oral and intestinal mucosa ulceration.

6. Each, isovaleric acidemia and 3-methylcrotonyl-CoA carboxylase deficiency were found in four individuals, which may indicate a considerably higher incidence of these diseases than previously reported.

7. In propranolol-pretreated dogs myocardial blood flow and coronary oxygen AV difference remained unaffected, suggesting that the coronary dilatory effect of metabolic acidemia involves beta adrenergic stimulation.

8. Many mutations have been found at the molecular genetic level over the past 20 years, and their implications for the limitation of enzyme activity of PCC in propionic acidemia are discussed.

9. Propionic acidemia is caused by a gene defect leading to malfunction of the enzyme propionyl–CoA carboxylase (PCC) and in turn to a pathologic accumulation of propionic acid.

10. Also disclosed is a method for treatment, amelioration or prophylaxis of a disease selected from the group consisting of phenylketonuria (PKU, Følling's disease), hyperphenylalaninemia (HPA), alcaptonuria (black urine disease), tyrosinemia, hypertyrosinemia, myasthenia gravis, histidinemia, urocanic aciduria, maple syrup urine disease (MSUD), isovaleric acidemia (isovaleryl-CoA dehydrogenase deficiency), homocystinuria, propionic acidemia, methylmalonic acidemia, and glutaric aciduria Type 1 (GA-I), galactosemia, comprising administering to the gastrointestinal tract of a patient in need thereof an effective amount of a composition of molecular imprinted polymers (MIPs), said composition being capable of binding a symptom provoking agent of said disease.

11. A new case of propionic acidemia is presented, paying special attention to the early symptoms of this disease, such as increased drowsiness, muscular hypotonia, poor feeding, hypothermia, metabolic acidosis, ketonuria and vomiting.

12. Propionic acidemia (PA) is a rare autosomal recessive disorder resulting from deficiency of the biotin-dependent enzyme propionyl-CoA carboxylase, which is necessary for the catabolism of branched chain amino acids and odd-chain fatty acids.

13. As an elevated incidence of deafness has been observed in patients with propionic acidemia, the question arises of whether mutations primarily responsible for this disease could also be the underlying cause for a genetic form of deafness.

14. The cardinal symptoms seen in classic homocystinuria are mental retardation, osteoporosis, myopia, and lens luxation. Methylenetetrahydrofolate reductase deficiency may present with psychomotor retardation, epilepsy, brain atrophy. Errors of Cbl metabolism account for metabolic crisis with methylmalonic acidemia.

15. We report on a 13 year old boy after bone marrow transplantation (BMT) who received total parenteral nutrition without vitamins. 15 days after BMT he experienced acute life threatening hyperlactic acidemia refractory to bicarbonate and tris. 100 mg thiamine i.v. resulted in a satisfactory clinical and biochemical response.

16. The data collected so far allow conclusions to be drawn for (a) tyrosinemia type I (TYR I) and (b) propionic acidemia, methylmalonic aciduria and vitamin B12 related disorders (PA/MMA/B12). (a) Succinylacetone (instead of the unspecific tyrosine) as the diagnostic metabolite marker for TYR I is derivatized to hydrazone and simultaneously analyzed with amino acids and acylcarnitines by electrospray ionization tandem mass spectrometry. (b) In newborns suspected of having PA/MMA/B12 due to elevated concentrations of propionylcarnitine (C3), methylmalonic acid (MMS) and 3-OH-propionic acid (3-OH-PS) were quantified in a second tier testing using the identical filter card by liquid chromatography tandem mass spectrometry. (a) Out of 480,000 newborns 3 were identified as having TYR I.