June 28 is the international day of phenylketonuria!
Phenylketonuria (PKU), a rare genetic disease caused by a mutation in the phenylalanine hydroxylase (PAH) gene, which causes a deficiency of the enzyme and an accumulation of the amino acid phenylalanine in the body. Metabolites formed as a result of the alternative breakdown of phenylalanine have a toxic effect on the child's nervous system and cause developmental delays, heart attacks and other pathologies.
For the diagnostics of phenylketonuria, "Synevo" offers "Baby Sensor 100+", which represents the possibility of non-invasive postnatal research of newborns and examines more than 100 congenital metabolic disorders.
Carry out laboratory tests and take advantage of a discount on the geneticist's online consultation!
To book an online consultation, follow the link: