Phenylketonuria

All proteins are composed of amino acids. There are 22 standard amino acids that, in multiple different combinations, form all the kinds of proteins in a human body and in other living organisms, including the plants and animals we eat.

Phenylalanine is one of the 22 amino acids and is found in varying degrees in nearly all kinds of proteins in our food. The human body cannot manufacture phenylalanine, so it must get this amino acid from food.

A gene in our DNA contains the instructions for the body to manufacture an enzyme called phenylalanine hydroxylase (PAH). This enzyme operates in the liver and the kidneys, and converts phenylalanine into tyrosine, another type of amino acid.

People who have a faulty version of the phenylalanine (PAH) gene cannot manufacture the PAH enzyme and therefore cannot break down phenylalanine. As a result, this amino acid accumulates in the body and causes damage to nerve cells in the body, especially the brain.

 

PKU is a recessive autosomal disorder. In these disorders, the affected person receives two faulty versions of the gene, one copy from each parent. If the person receives one faulty allele and one working allele, that person is a healthy carrier of the gene. Healthy carriers do not suffer from the disorder, but can pass on the faulty allele to their offspring.

Phenylketonuria causes a toxic build-up of phenylalanine. 

Several mutations can affect the PAH gene. Some of these mutations result in a PAH enzyme that is faulty but partially active, resulting in a milder form of PKU. Other mutations render the PAH enzyme completely useless, resulting in 'classic' PKU, a severe disorder.

Types

As mentioned above, the PAH gene can be completely or partially faulty. Thus, PKU can also be classified as severe, moderate or mild.

Signs and symptoms

Babies born with PKU show no symptoms at birth. If PKU is not detected and/or the recommended diet is not followed within a few weeks after birth, symptoms will gradually start to appear, as phenylalanine starts accumulating.

The most profound symptom of PKU is intellectual disability. This can be mild to severe according to the severity of the genetic disorder. Problems can include:

• Learning difficulties;
• Behavioral disorders, such as hyperactivity and self-harm, and;
• Epilepsy.

Other symptoms that can appear as phenylalanine accumulates in the child's body include:

• An unusually small head (microcephaly);
• Jerky movements, trembling and seizures;
• A distinctive musty smell of the body, breath and urine;
• Recurrent vomiting;
• Eczema, and;
• Light-colored skin, fair hair, and light-colored (often blue) eyes.

Children and adults with PKU who stick to their diet are generally fine and function normally throughout their lifetime.

There are indications that adults with PKU might have a somewhat higher chance of developing certain mental health problems, such as depression and anxiety, and some minor problems with cognitive skills such as planning.

PKU and pregnancy

A woman with PKU can, if she does not follow the diet, cause severe problems for her offspring. The phenylalanine in her blood can affect the fetus' development in the womb and cause it to have severe cognitive problems.

Methods for diagnosis

A blood test for PKU is performed on all newborn babies. If the result is positive, further blood tests and urine tests are done to confirm the diagnosis.

Types of treatment

The only treatment for PKU is a special diet low in phenylalanine that must be followed for life. The diet is not easy to follow, as it is quite strict and requires effort and discipline. In milder cases of PKU, a measure of leeway is sometimes possible. A person with PKU will normally undergo regular testing for phenylalanine levels. The test results will inform about the compliance with the special diet.

It is particularly important for women to follow the diet strictly before and during pregnancy, as the phenylalanine that accumulates in their bodies will cause profound harm to their unborn baby.

Future treatment prospects

In the future, gene therapy may be able to cure PKU. This, however, is still some way off.

An enzyme, PEGylated recombinant phenylalanine ammonia lyase (PEG-PAL), which may replace PAH and break down phenylalanine in the body has been in development for some years and is showing promise, but is still not approved for use at this time.

Prognosis

If PKU is diagnosed and managed properly (i.e. the diet is followed, which is not an easy diet to follow) then you can live with PKU with no ill effects.

Prevention

People who have a family history of PKU can consider genetic counselling before attempting to conceive babies, to assess their chances of having children with PKU.

Women with PKU can prevent birth defects in their babies by adhering to the restricted diet before and during pregnancy.