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Codigo Baby

Your genetic report helps you to know if your baby carries any risk of developing metabolic and congenital diseases.

$3,500 MXN

What study covers the report?

Codigo Baby          $3,500 MXN

How does it work?

It provides you with genetic information about your baby’s genetics so that you know his predisposition to metabolic and congenital diseases. This study will give your baby´s doctor the opportunity to establish timely treatments for your baby and know the risks associated with each disease.

We study your baby’s predisposition to different congenital and metabolic diseases.

Based on the genotype of your baby as well as the hereditary patterns of the diseases analyzed, we give you information about your baby’s predisposition to experience various metabolic and congenital diseases. With this information, you and your doctor can establish an appropriate preventive plan.
What genetic diseases does the new born screening Codigo Baby include?

Our Codigo Baby genetic screen includes markers for the following diseases:
Glutaric aciduria type 1
Glutaric aciduria type 2
Propionyl-CoA carboxylase deficiency
Alpha thalassemia
Beta thalassemia
Carnitine deficiency, systemic primary
Combined malonic and methylmalonic aciduria
Phenylketonuria
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyltransferase I deficiency
Homocystinuria
Hyperphenylalaninemia
Very long chain acyl-CoA dehydrogenase deficiency
Hypermethioninemia
Holocarboxylase synthetase deficiency
Argininosuccinate lyase deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Deficiency of UDP glucose-hexose-1-phosphate uridylyltransferase
Citrullinemia
Trifunctional protein deficiency
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Deficiency of 2-methylbutyryl-CoA dehydrogenase
Carnitine acylcarnitine translocase deficiency
Deficiency of butyryl-CoA dehydrogenase
Deficiency of isobutyryl-CoA dehydrogenase
Galactosemia
3 Methylcrotonyl-CoA carboxylase 1 deficiency
Biotinidase deficiency
Congenital adrenal hyperplasia
Cystic fibrosis
Congenital hypothyroidism
Glucose 6 phosphate dehydrogenase deficiency
Methylmalonic aciduria
Maple syrup urine disease
Sickle cell anemia
Tyrosinemia

What is my baby’s report?

Our test includes a statistical analysis of the risk of several multifactorial diseases according to the presence of different genetic markers in your baby’s genotype. In addition, your baby’s report includes information on genetic variants of high genetic risk variants associated with a large number of congenital diseases.

The most advanced genetic test in Latin America

Check out our full package and discover even more about yourself and your loved ones.

We are the healthiest
option in genetic analysis

Find out about new discoveries and technological advances

(222) 9501952 / (222) 9501989

contacto@codigo46.com.mx

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Oficinas. Periférico Ecológico #3507 Int.1609 Reserva Territorial Atlixcayotl. San Andrés Cholula, Puebla

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