#Aminoacidopathies
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Genes Tests
Tyrosinemia Type I Screening
Tyrosinemia Type I is a rare genetic disorder that affects the liver’s ability to break down tyrosine, an amino acid.…
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Genes Tests
Homocystinuria Screening
What is Homocystinuria Screening? Homocystinuria screening is a genetic test to detect a rare metabolic disorder called homocystinuria. This condition…
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Genes Tests
Phenylketonuria (PKU) Screening
What is Phenylketonuria (PKU) Screening? Phenylketonuria (PKU) screening is a mandatory test performed on newborns to detect the presence of…
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