Phenylketonuria Sentence Examples

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

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

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

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

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

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.

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

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.

Phenylketonuria (PKU) is a rare metabolic disorder caused by a deficiency in the production of the hepatic (liver) enzyme phenylalanine hydroxylase (PAH).

Every state in the United States has mandatory newborn screening programs in place for phenylketonuria, as well as other diseases.

Autism has also been shown to occur more frequently among individuals who have certain medical conditions, including fragile X syndrome, tuberous sclerosis, congenital rubella syndrome, and untreated phenylketonuria.

People with phenylketonuria (PKU) should consult a physician before taking this medicine.

Hypothyroidism and phenylketonuria (PKU) are two common metabolic conditions that may be present at birth.

Women who are at risk of phenylketonuria (PKU) should not take aspartame because it can increase the amount of the amino acid phenylalanine, which can harm the developing baby.

For example, a small percentage of people must keep the phenylalanine that they take in at a very low level because of a disease called Phenylketonuria.

Several dangers of phenylalanine supplements should be noted, especially for people with a genetic disorder called phenylketonuria (PKU).

Phenylketonuria is a genetically inherited disease in which people cannot process the amino acid phenylalanine.

These include Phenylketonuria, Williams Syndrome, Tuberous Sclerosis, and Fragile X syndrome.

Low- or no-calorie sweeteners are fine for everyone to use as a substitute for sugar, except for those with a condition known as phenylketonuria, who should not consume aspartame.