#NewbornScreening
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Genes Tests
Methylmalonic Acidemia (MMA) Screening
What is Methylmalonic Acidemia (MMA) Screening? Methylmalonic acidemia (MMA) is a rare genetic disorder that affects the body’s ability to…
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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
Biotinidase Deficiency Screening
What is Biotinidase Deficiency Screening ? Biotinidase deficiency screening is a newborn screening test that checks for a rare genetic…
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Genes Tests
Maple Syrup Urine Disease (MSUD) Screening
What is Maple Syrup Urine Disease (MSUD) Screening? Maple Syrup Urine Disease (MSUD) is a rare genetic disorder that affects…
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Genes Tests
Cystic Fibrosis Screening
What is Cystic Fibrosis Screening? Cystic Fibrosis (CF) screening is a genetic test used to identify carriers of the CF…
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Genes Tests
Sickle Cell Disease Screening
What is Sickle Cell Disease Screening? Sickle Cell Disease (SCD) screening is a genetic test to determine if a person…
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Genes Tests
Galactosemia Screening
What is Galactosemia Screening ? Galactosemia screening is a newborn screening test that checks for a rare genetic disorder called…
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Genes Tests
Hypothyroidism Screening
What is Hypothyroidism Screening? Hypothyroidism screening is a medical test used to detect low levels of thyroid hormone in the…
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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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