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 causes delayed mental and social skills, below average head size, hyperactivity, skin rashes, seizures, tremors, and intellectual disability.
The best treatment of phenylketonuria is a diet that is extremely low in phenylalanine during childhood. A person can also take fish oil supplements and iron supplements to help treat some of the symptoms.
phenylketonuria
phenylketonuria
Phenylketonuria
2.42% of the world's population has Phenylketonuria (pku)
PKU
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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 genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway
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