Clinical Services

PKU (PHENYLKETONURIA)

PKU (PHENYLKETONURIA)

ACCEPT:

  • If there is no intellectual deficit and the condition is controlled by diet and supplements only

ADDITIONAL INFORMATION

Phenylketonuria (PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a building block of proteins that is obtained through the diet. It is found in all proteins and in some artificial sweeteners. If PKU is not treated, phenylalanine can build up to harmful levels in the body, causing intellectual disability and other serious health problems. The signs and symptoms vary from mild to severe. The most severe form of this disorder is known as classic PKU. Infants with classic PKU appear normal until they are a few months old. Without treatment, these children develop permanent intellectual disability. Seizures, delayed development, behavioral problems, and psychiatric disorders are also common

PKU cannot be transmitted by blood transfusion therefore there is no risk to recipient safety

IBTS/MEDD/DSGDE/0001Attachment 4.376Ver 1.1

 

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