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Galactosemia is a genetic disorder which is caused by a lack of the GALT enzyme. This is essential in breaking down the milk sugar galactose.
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DNA encodes enzymes so it is possible for an individual to have a genetic disorder that causes them to lack a specific enzyme?
True.
Is Lactose intolerance dominant or recessive trait?
Galactosemia is an autosomal recessive trait.
The enzyme salivary amylase will act on starch but not on protein?
Lack protein.
What enzyme breaks down corn?
Digestive enzymes are enzymes that break down food into usable energy. The digestive enzyme that breaks down corn is called xylanese. Humans lack this enzyme.
What causes enzyme specificity?
The enzyme's surface folds are complementary to the substrate's surface folds.
How are the newborn babies controlled for galactosemia?
Galactosemia occurs when an enzyme, called 'galactose-1-phosphate uridyl transferase' (GALT) is either missing or not working properly so the children are examined carefully for this enzyme
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.
Galactosemia is the name of a metabolic disorder In this disorder an enzyme is missing that is needed to?
...that is needed to break down galactose.
DNA encodes enzymes so it is possible for an individual to have a genetic disorder that causes them to lack a specific enzyme?
True.
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.
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.
Is Lactose intolerance dominant or recessive trait?
Galactosemia is an autosomal recessive trait.
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 people are lack tose and tolarant?
lactose intolerant. they lack the enzyme amylase which digests dairy
What does the medical abbreviation PKU mean?
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Why can't humans digest wood?
Because they lack an enzyme
