galactosemia造句

• Without treatment, mortality in infants with galactosemia is about 75 %.
• A person with galactosemia doesn't have one of these enzymes.
• The routine NBS is accurate for detection of galactosemia.
• This is largely due to a lack of functional animal models of classic galactosemia.
• Galactosemia is sometimes confused with lactose intolerance, but galactosemia is a more serious condition.
• Galactosemia is sometimes confused with lactose intolerance, but galactosemia is a more serious condition.
• Carriers show no symptoms of galactosemia.
• Studies of Type III galactosemia symptoms are mostly descriptive, and precise pathogenic mechanisms remain unknown.
• Because early intervention is key, galactosemia is included in newborn screening programs in many areas.
• Approximately 70 % of galactosemia-causing alleles have a single missense mutation in exon 6.
• The Beutler's test screens for galactosemia by detecting the level of enzyme of the infant.
• Duarte galactosemia is a milder form of classical galactosemia and usually has no long term side effects.
• Duarte galactosemia is a milder form of classical galactosemia and usually has no long term side effects.
• Treatment of galactosemia is most successful if initiated early, and includes dietary restriction of lactose intake.
• Galactosemia can even be detected through NBS before any ingestion of galactose-containing formula or breast milk.
• Galactosemia is caused by mutations in the gene that makes the enzyme galactose-1-phosphate uridylyltransferase.
• Dietary reduction of galactose is also the treatment but not as severe as in patients with classical galactosemia.
• Dosage is reduced in case of galactosemia as most preparations contain the monosaccharide galactose due to its synthesis process.
• At present, California tests newborn blood samples for PKU, galactosemia, primary congenital hypothyroidism and sickle cell anemia.
• Most also routinely test for galactosemia, a rare inherited disorder in which the body can't metabolize sugar.