Phenylketonuria sentence example

phenylketonuria
  • Phenylketonuria is a genetic disorder, which means, from birth, these persons cannot break down the amino acid phenylalanine.
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  • The classic example of this is in the disorder called phenylketonuria (PKU ).
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  • Despite developing phenylketonuria during his childhood years his mother Mary encouraged him to paint at the age of twenty-four.
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  • However, it is important to note that infants suffering from the rare genetic disease phenylketonuria (PKU) should not consume aspartame.
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  • 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.
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  • Phenylketonuria, Tay-Sachs disease, and galactosemia are inborn errors of metabolism.
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  • 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.
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  • Women with diabetes and phenylketonuria (an inherited liver condition also called PKU) are at higher risk of having children with congenital heart defects.
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  • 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.
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  • Phenylketonuria (PKU) is a rare metabolic disorder caused by a deficiency in the production of the hepatic (liver) enzyme phenylalanine hydroxylase (PAH).
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  • Every state in the United States has mandatory newborn screening programs in place for phenylketonuria, as well as other diseases.
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  • 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.
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  • People with phenylketonuria (PKU) should consult a physician before taking this medicine.
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  • Hypothyroidism and phenylketonuria (PKU) are two common metabolic conditions that may be present at birth.
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  • 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.
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  • 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.
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  • Several dangers of phenylalanine supplements should be noted, especially for people with a genetic disorder called phenylketonuria (PKU).
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  • Phenylketonuria is a genetically inherited disease in which people cannot process the amino acid phenylalanine.
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  • These include Phenylketonuria, Williams Syndrome, Tuberous Sclerosis, and Fragile X syndrome.
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  • 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.
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