Examples of 'phenylketonuria' in a sentence
Meaning of "phenylketonuria"
Phenylketonuria is a genetic disorder characterized by the body's inability to process an amino acid called phenylalanine, leading to a buildup of this substance in the body which can cause intellectual disabilities and other health problems
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- A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine.
How to use "phenylketonuria" in a sentence
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phenylketonuria
May be harmful for people with phenylketonuria.
Phenylketonuria intellectual disability.
It may be harmful for patients with phenylketonuria.
Patient suffering from phenylketonuria should not use the product.
Activities for children suffering from phenylketonuria.
If you have phenylketonuria you should avoid using this product.
It is used with a special diet to treat phenylketonuria.
They also suffered from phenylketonuria and renal tubular dysfunction.
It is also beneficial for people with phenylketonuria.
Women affected by phenylketonuria by themselves do not risk additional complications during pregnancy.
Avoid taking by people suffering from phenylketonuria.
All children are screened for phenylketonuria and hypothyroidism before discharge from hospital.
Therefore it may be harmful for people with phenylketonuria.
The screening enabled the detection of phenylketonuria in three and hypothyroidism in two cases.
He was also involved in the development of treatments for phenylketonuria.
See also
Screening for phenylketonuria.
For instance elevated phenylalanine levels can indicate phenylketonuria.
Loss of intellectual function in children with phenylketonuria after relaxation of dietary phenylalanine restriction.
Diet for children after a year with phenylketonuria.
Children and pregnant women with phenylketonuria are provided with free medicinal nutrition mixtures.
A mutation in a single gene causes phenylketonuria.
People with phenylketonuria are advised to stay away from foods with high phenylalanine content.
Prospective study of early neonatal screening for phenylketonuria.
A syndrome called Phenylketonuria is also managed through diet.
Monitoring phenylalanine in patients with phenylketonuria.
Phenylketonuria or PKU is a metabolic error that a child is born with.
Programme on early detection of phenylketonuria.
Phenylketonuria is the most manageable metabolic condition and I am grateful for that.
Dating someone with phenylketonuria.
PKU or Phenylketonuria is a genetically inherited condition.
Your child has phenylketonuria.
One example of enzyme deficiency is the most common type of phenylketonuria.
See also Phenylketonuria.
Should be avoided by those with the genetic disorder phenylketonuria.
Phenylketonuria ( pku ) is a recessive autossomic disease resultant of pah deficiency.
This medicine should be used with caution in patients with phenylketonuria.
If you suffer from phenylketonuria a rare, hereditary disorder of the metabolism.
All newborns have been undergoing screening examinations for hypothyreosis and phenylketonuria.
If phenylketonuria is picked up, further tests will be arranged to confirm the diagnosis.
This substance may be harmful for people with phenylketonuria a metabolic disease.
Do not take patients with phenylketonuria ( a serious hereditary disease leading to impaired mental development ).
Aspartame is a source of phenylalanine which may be harmful for people with phenylketonuria.
This substance may be harmful for people with phenylketonuria ( a rare metabolic disease ).
Tomorrow we will have eradicated genetic diseases such as mucoviscidosis and phenylketonuria.
This is a concern if you have a disorder called phenylketonuria ( a problem with amino acids ).
Another objective is to control the phenylalanine levels in the patients with phenylketonuria.
Deglutinate food for children with celiac disease and phenylketonuria ( concentrates and readyforconsumption products ) ;.
Environment plays a major role in effects of the human genetic disease phenylketonuria.
Certain diseases, such as phenylketonuria and homocystinuria, cause chronic neurological damage without acute decompensation.
This medicine contains phenylalanine and may be harmful for people with phenylketonuria.
