galactosemia
IPA: gʌɫˈæktoʊsˈimiʌ
noun
- (medicine) A genetic metabolic disorder characterized by an inability to metabolize galactose properly
- The presence of galactose in the blood
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Examples of "galactosemia" in Sentences
- Severe form is similar to galactosemia.
- A simple spot screening test for galactosemia.
- Types of Galactosemia and the Prevalence of Cataract.
- Email: galactosemia. ureach.com www. galactosemia.com
- However, the rarity of galactosemia is a serious issue.
- Treatment for Galactosemia and the Galactosemic Cataract.
- Galactosemia is a childhood disease of hereditary nature.
- The routine NBS is accurate for detection of galactosemia.
- A person with galactosemia doesn't have one of these enzymes.
- The pathophysiology of galactosemia has not been clearly defined.
- A new method for the detection of galactosemia and its carrier state.
- Galactosemia is normally first detected through newborn screening, or NBS.
- These conditions include sickle cell anemia, beta thalassemia, phenylketonuria PKU, hypothyroidism,8 and galactosemia.
- The baby can not breastfeed: The child has a birth defect or inborn errors of metabolism such as galactosemia that makes breastfeeding difficult or impossible.
- Some disorders, such as galactosemia, are initially screened on a blood spot with subsequent confirmation in red blood cells or plasma using quantitative techniques.
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- In addition, the laboratory offers a specialist expertise in the diagnosis of lysosomal, galactosemia and fatty acid oxidation enzyme defects for which diseases the laboratory has a National and International reputation.
- People who have a G6PD deficiency have the following symptoms: pale skin fatigued and tired rapid and shallow breathing abnormal/rapid heartbeat enlarged spleen yellowish tint to eyes galactosemia which is found in babies.