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What causes galactosemia II?
Galactosemia II is caused by defects in both copies of the gene that codes for an enzyme called galactokinase (GALK). The frequency of occurrence of galactosemia II is about one in 100,000-155,000 births.
Did Mel Gibson have galactosemia?
No, Mel Gibson does not have galactosemia. Galactosemia is a rare genetic disorder that affects the body's ability to process galactose, a sugar found in milk and dairy products. There is no public information or credible sources indicating that Gibson has been diagnosed with this condition.
What health condition is Galactosemia?
The health condition galactosemia occurs when the body has a deficiency in processing glucose. The condition mostly affects infants and can be life threatening if not treated.
What can be treated by placing the affected individual on a restricted diet that excludes dairy products huntington disorder down syndromefaulty-enamel trait or galactosemia?
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
Why does congenital galactosemia appear only into infants?
Galactosemia is a condition where infants have trouble digesting lactose to the point where it could harm their organs. People's systems get stronger as people age so older children are no longer affected by the condition.
What causes Galactosemia?
Galactosemia is a very rare disease that is received through a recessive trait. It is hardly diagnosed but can also be very easily confused with lactose intolerance. Though the two can be very similar but they are very different. Galactosemia is when your body cannot process galactose and lactose intolerance is when your body cannot process lactose. Lactose and galactose can be found in generally the same food group, dairy. The very important difference between the two is that lactose intolerance causes the symptoms of gas, cramps and diarrhea and galactosemia causes excess fat to build up in the brain, cause mental retardation and finally death.
What do galactosemia and tay-sachs disease have in common?
Both galactosemia and Tay-Sachs disease are genetic disorders caused by the absence or dysfunction of a particular enzyme. Galactosemia is a disorder where the body is unable to break down galactose, a sugar found in milk, while Tay-Sachs disease is a disorder where the body lacks an enzyme needed to break down certain lipids in the brain. Both conditions can lead to serious health complications if not managed properly.
Is there reserch into gene therapy for galactosemia?
yes
With galactosemia what does the Los Angeles gene refer to?
the city
What type Galactosemia is sever or most sever?
sever type1 classic is the most sever type,....... sever type1 (classic): galactosemia is the most sever galactosemic disorder
What does the medical abbreviation PKU mean?
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Like many genetic disorders galactosemia is a disruption of a metabolic pathway due to a malfunctioning?
Many genetic orders such as galactosemia is a disruption in a metabolic pathway. Galactosemia is a disruption in the process of breaking down galactose.
