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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 are the symptoms of galactosemia?
galactosemia is a rare congenital disease in infants, inherited as an autosomal recessive disorder.here galactose metabolism is impaired leading to increased galactose levels in circulation and urine.the clinical symptoms areloss of weight(in infants). hepatosplenomegalyjaundicemental retardationin severe cases- cataract, amino aciduria and albuminuria are observed.
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 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.
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.
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 does the medical abbreviation PKU mean?
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How many babies died on board the titanic?
Titanic had 34 infants sailing on her maiden voyage that were two or younger. Of them, 13 died.
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.
How many babes were on the titanic?
34 infants sailing on Titanic were two or younger. 21 survived, 13 died.
Is Lactose intolerance dominant or recessive trait?
Galactosemia is an autosomal recessive trait.
Is there reserch into gene therapy for galactosemia?
yes
