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.
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
Galactosemia is primarily caused by mutations in the GALT gene, which encodes an enzyme called galactose-1-phosphate uridylyltransferase. Mutations in this gene result in reduced or absent enzyme activity, leading to the accumulation of galactose-1-phosphate in the body.
The probability that a child is affected with galactosemia is 1/40,000. The probability that both children are affected would be (1/40,000) * (1/40,000) = 1/1,600,000,000.
No, if one parent is a carrier of galactosemia and the other parent is not, the child has a 50% chance of being a carrier as well. It only requires one parent to pass on the gene for the child to be a carrier.
Galactosemia is a rare genetic metabolic disorder, in which an individual (usually an infant) lacks the enzyme GALT, which breaks down the sugar galactose in the body. Since galactoseis produced by the breakdown of lactose (in milk) into glucose, this sugar rapidly accumulates in the body, and may result in damage to the kidneys, liver, eyes, and brain.(see the related link)
The lack of the enzyme galactose-1-phosphate uridyltransferase (GALT) causes galactosemia. This enzyme is responsible for the breakdown of galactose in the body, and its deficiency leads to the accumulation of galactose and its toxic byproducts.
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.
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.
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
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.
Galactosemia is primarily caused by mutations in the GALT gene, which encodes an enzyme called galactose-1-phosphate uridylyltransferase. Mutations in this gene result in reduced or absent enzyme activity, leading to the accumulation of galactose-1-phosphate in the body.
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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.
the city
it was found in 1908 by Von Ruess
sever type1 classic is the most sever type,....... sever type1 (classic): galactosemia is the most sever galactosemic disorder