Genes Tests
Genes Cure Tests offer advanced genetic testing solutions tailored to help you understand your unique health profile. From detecting inherited conditions to personalized wellness insights, our tests empower you with knowledge to make informed health decisions. Trust Genes Cure for reliable, accurate results that bring clarity to your genetic health journey.
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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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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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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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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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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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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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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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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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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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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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