Examples of 'galactosemia' in a sentence
Meaning of "galactosemia"
galactosemia (noun) - a rare genetic disorder that affects the body's ability to metabolize galactose, a sugar found in milk and dairy products, leading to potentially severe health problems if left untreated
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- A genetic metabolic disorder characterized by an inability to metabolize galactose properly
- The presence of galactose in the blood
How to use "galactosemia" in a sentence
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galactosemia
Not appropriate for children with galactosemia.
Galactosemia is inherited as an autosomal recessive trait.
Researchers have identified several types of galactosemia.
Your infant has galactosemia symptoms.
Among those suffering are children with galactosemia.
Galactosemia is a rare genetic disorder.
Fertility preservation in female classic galactosemia patients.
Galactosemia is an inability to break down the milk sugar galactose.
Not for people with galactosemia.
Galactosemia is an autosomal recessive inherited disorder detectable in newborns and childhood.
It is thus the fragment preferably used in diagnosis of galactosemia.
If you have a family history of galactosemia and are considering having children.
Nor does it teach a method of diagnosing galactosemia.
Galactosemia is hereditary.
One example of this is galactosemia.
See also
Galactosemia not infrequently accompanies resistant ovary syndrome and may be a causative factor.
Severe form is similar to galactosemia.
Girls with galactosemia may require hormone treatment when they reach puberty.
Carriers show no symptoms of galactosemia.
Patients with galactosemia and lactase deficiency should consider that the drug contains lactose.
Metabolic disorders such as galactosemia.
Infants with galactosemia who are not treated shortly after birth can develop permanent effects.
Metabolic factors such as galactosemia.
The treatment for galactosemia is to restrict galactose and lactose from the diet for life.
Many states have mandatory screening of newborns for galactosemia.
Symptoms of Duarte galactosemia are much less severe.
Several methods exist for neonatal screening for galactosemia.
Newborns with galactosemia I begin to show symptoms as soon as they begin to drink milk.
This is largely due to a lack of functional animal models of classic galactosemia.
Infants are routinely screened for galactosemia in the United States.
An example of this would be a baby who had the genetic disease galactosemia.
Prevention of Galactosemia.
In a preferred embodiment the invention provides a novel method of screening for galactosemia.
Those disorders are phenylketonuria, galactosemia and fructose intolerance.
Today we had the blood test done to see if we are carriers of galactosemia.
Galactosemia results from an inability to process galactose, a simple sugar.
Further tests will be ordered to determine which type of galactosemia your child has.
Babies with galactosemia must be fed a non-dairy formula.
Newborn screening tests detect most babies with galactosemia soon after birth.
Babies with classic galactosemia may have liver problems, malnutrition, or mental retardation.
The inventors have developed a novel test applicable to neonatal screening for galactosemia.
The most common treatment for galactosemia is a low-galactose diet.
GALE is only one type of a broader condition group called galactosemia.
Galactosemia is a condition with multiple forms, each of which have different causes and outcomes.
Also those babies who suffer lactose intolerance or galactosemia can have soy milk formula.
A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemia.
Learn more about Galactosemia.
Individuals with galactosemia can not tolerate any form of milk, including human breast milk.
Most infants in the US are screened for galactosemia at birth.
Since children with galactosemia can not consume milk products, their calcium levels may be too low.
