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Phenylketonuria – ADVENTIA Carrier Screening

June 28 is World Phenylketonuria Day!
Phenylketonuria (PKU) is a rare inherited disease caused by a mutation in the phenylalanine hydroxylase (PAH) gene, which leads to the accumulation of the amino acid phenylalanine in the body.
Accumulation of phenylalanine causes developmental delays and many other problems in children.

ADVENTIA Genetic Disease Carrier Screening Focus Panels investigate the carrier status of phenylketonuria and other genes:

Adventia – full panel (1 person)

 

 

Adventia – full panel (2 person)

 

 

 

Adventia – basic panel (1 person)

 

Learn more 

Adventia – basic panel (2 person)

 

Learn more 

 

 

 

 

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