Phenylketonuria (PKU) is a genetic metabolic disorder that increases levels of the essential amino acid known as phenylalanine in the blood. People with PKU are unable to metabolize phenylalanine ...
PKU is a genetic disease that manifests at birth and results from an inability to break down phenylalanine (phe), an amino acid that is commonly found in many foods. Left untreated, high levels of ...
PKU is a rare genetic disease that manifests at birth and is marked by an inability to break down phenylalanine (phe), an amino acid that is commonly found in many foods. Left untreated ...
Inborn Errors of Metabolism (IEMs) are a class of rare genetic disorders that disrupt the body’s ability to convert food into energy. This process is crucial for various biological functions, ...