Phenylketonuria (PKU) is an inborn error in metabolism that prevents the body from using phenylalanine, an amino acid necessary for normal growth and development.
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.
Phenylketonuria is a very rare condition where amino acids are not properly broken down. This condition is something that someone is born with.
phenylketonuria
Phenylketonuria is an autosomal recessive genetic disorder. This means that an individual must inherit two copies of the defective gene (one from each parent) in order to develop the condition.
phenylketonuria
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.
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.
It is possible for a parent with phenylketonuria to pass the condition to their offspring if both parents are carriers of the PKU gene mutation. In this case, there is a 25% chance that their child will inherit two copies of the mutated gene and develop phenylketonuria. Genetic testing can provide more information on the risk of passing PKU to offspring.
2.42% of the world's population has Phenylketonuria (pku)
Phenylketonuria
A genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as Phenylketonuria (PKU). This leads to a buildup of phenylalanine in the body, which can be toxic to the brain if not managed properly through a restricted diet low in phenylalanine.
PKU