चयापचय का एक अनुवांशिक विकार; एंजाइम की कमी को शरीर के तरल पदार्थ में फेनिलालाइनाइन के संचय में टायरोसिन के परिणामों में फेनिलालेनिन की आवश्यकता होती है जो मानसिक कमी की विभिन्न डिग्री का कारण बनती है

phenylketonuria's Usage Examples:

Selenium supplements are not normally required except in children with phenylketonuria receiving a low-protein diet, although it may sometimes be associated with thyroid problems.

Women with diabetes and phenylketonuria (an inherited liver condition also called PKU) are at higher risk of having children with congenital heart defects.

Phenylketonuria (PKU)-A rare, inherited, metabolic disorder in which the enzyme necessary to break down and use phenylalanine, an amino acid necessary for normal growth and development, is lacking.

Phenylketonuria, Tay-Sachs disease, and galactosemia are inborn errors of metabolism.

Single gene defects such as phenylketonuria (PKU) and other inborn errors of metabolism may also cause mental retardation if they are not found and treated early.

phenylketonuria screening methods.

However, it is important to note that infants suffering from the rare genetic disease phenylketonuria (PKU) should not consume aspartame.

Despite developing phenylketonuria during his childhood years his mother Mary encouraged him to paint at the age of twenty-four.

The classic example of this is in the disorder called phenylketonuria (PKU ).

Phenylketonuria is a genetic disorder, which means, from birth, these persons cannot break down the amino acid phenylalanine.

phenylketonuria's Meaning':

a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency