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Is an inherited autosomal recessive disorder in which a person lacks the enzyme that is necessary to break down the amino acid phenylalanine phenylalanine then breaks down to form chemicals that?
PKU!
In phenylketonuria what amino acid becomes conditionally essential?
In phenylketonuria, the amino acid phenylalanine becomes conditionally essential. This is because the body is unable to break down phenylalanine properly, leading to an accumulation of phenylalanine in the blood and potentially toxic levels in the brain. Dietary restriction of phenylalanine is necessary to prevent health complications in individuals with phenylketonuria.
What is an inherited autosomal recessive disorder of the blood in which a person lacks the enzyme that is necessary to break down the amino acid phenylalanine then breaks down to form chemicals that?
Phenylketonuria (PKU) is an inherited autosomal recessive disorder caused by a deficiency of the enzyme phenylalanine hydroxylase. This enzyme is necessary to break down the amino acid phenylalanine. Without this enzyme, phenylalanine accumulates in the body and can lead to the formation of harmful byproducts that can cause intellectual disability and other complications. Treatment involves a strict low-phenylalanine diet to prevent these complications.
Infants with PKU cannot break down the amino acid?
Phenylalanine. This can lead to a build-up of phenylalanine in the blood, causing brain damage and intellectual disabilities if left untreated. Infants with PKU require a special diet low in phenylalanine to prevent these complications.
How does PKU impact protein synthesis?
PKU (phenylketonuria) is a genetic disorder that affects the enzyme needed to break down the amino acid phenylalanine. Without this enzyme, phenylalanine can build up to harmful levels in the blood and impair protein synthesis. The excess phenylalanine can also lead to decreased levels of other amino acids, affecting overall protein production in the body.
Is an inherited autosomal recessive disorder in which a person lacks the enzyme that is necessary to break down the amino acid phenylalanine phenylalanine then breaks down to form chemicals that?
PKU!
What are the possible symptoms to phenylalanine?
Phenylalanine is an amino acid. When someone is unable to break phenylalanine down, the condition is called Phenylketonuria. Phenylketonuria is usually diagnosed in newborn babies. Symptoms of phenylketonuria are seizures, tremors, small head size, delayed mental and social skills, and skin rashes.
In phenylketonuria what amino acid becomes conditionally essential?
In phenylketonuria, the amino acid phenylalanine becomes conditionally essential. This is because the body is unable to break down phenylalanine properly, leading to an accumulation of phenylalanine in the blood and potentially toxic levels in the brain. Dietary restriction of phenylalanine is necessary to prevent health complications in individuals with phenylketonuria.
What is an inherited autosomal recessive disorder of the blood in which a person lacks the enzyme that is necessary to break down the amino acid phenylalanine then breaks down to form chemicals that?
Phenylketonuria (PKU) is an inherited autosomal recessive disorder caused by a deficiency of the enzyme phenylalanine hydroxylase. This enzyme is necessary to break down the amino acid phenylalanine. Without this enzyme, phenylalanine accumulates in the body and can lead to the formation of harmful byproducts that can cause intellectual disability and other complications. Treatment involves a strict low-phenylalanine diet to prevent these complications.
Infants with PKU cannot break down the amino acid?
Phenylalanine. This can lead to a build-up of phenylalanine in the blood, causing brain damage and intellectual disabilities if left untreated. Infants with PKU require a special diet low in phenylalanine to prevent these complications.
What causes pku?
PKU or phenylketonuria is caused by mutations in the gene that helps make an enzyme called phenylalanine hydroxylase or PAH. This enzyme is needed to convert the amino acid phenylalanine into other forms that the body uses and needs. When this gene is mutated the body can't break down foods that are high in protein such as milk, cheese, nuts, or meat.
How does PKU impact protein synthesis?
PKU (phenylketonuria) is a genetic disorder that affects the enzyme needed to break down the amino acid phenylalanine. Without this enzyme, phenylalanine can build up to harmful levels in the blood and impair protein synthesis. The excess phenylalanine can also lead to decreased levels of other amino acids, affecting overall protein production in the body.
What is a condition which makes it impossible to metabolize certain proteins?
Phenylketonuria (PKU) is a condition that makes it impossible to metabolize the amino acid phenylalanine. People with PKU lack an enzyme called phenylalanine hydroxylase, which is required to break down phenylalanine. If left untreated, the buildup of phenylalanine can lead to brain damage and other neurological problems, so individuals with PKU must follow a strict low-phenylalanine diet.
What do proteins break into?
proteins break into amino acids ;)
Lysomes use their enzymes to break proteins into?
The lysosomes break proteins into Amino Acids
What does your digestive system break proteins into?
amino acids
What do protease break down into?
Protease is an enzyme so it would break down into amino acids. (If you meant protein then the same is true)
