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It is essential to perform newborn screening tests in order to identify any conditions or congenital diseases before symptoms become apparent, and provide the appropriate treatment as soon as possible.

Dedos del pie del bebé

Ensure the health of your baby



We run laboratory tests from blood taken from the baby’s heel, to promply detect any metabolic diseases that do not show symptoms and to be able to provide treatment reducing the damage, such as: intellectual disability, delayed growth and death.


Ideally between the third and fifth day after birth, up to 30 days.


  1. Congenital hypothyroidism

  2. Hyperthyrotropinemia

  3. Congenital adrenal hyperplasia salt-losing variety

  4. Congenital adrenal hyperplasia simple virilizing variety

It detects 4 diseases

Price: $  MXN370

It detects 18 diseases

Price: $ 650 MXN


  1. Congenital hypothyroidism

  2. Hyperthyrotropinemia

  3. Congenital adrenal hyperplasia salt-losing variety 

  4. Congenital adrenal hyperplasia simple virilizing variety

  5. Hemoglobin S- Sickle Cell Anemia

  6. Hemoglobin C disease

  7. Hemoglobin SC disease

  8. Hemoglobin E disease

  9. Hemoglobin D disease

  10. Sickle Cell Beta Thalassemia disease

  11. Hemoglobin C-Beta Thalassemia disease

  12. Hemoglobin E-Beta Thalassemia disease 

  13. Hemoglobin H disease

  14. Hemoglobin S-Alpha Thalassemia disease

  15. Hemoglobin SC- Alpha Thalassemia disease

  16. Hemoglobin G trait 

  17. Hemoglobin G-Alpha Thalassemia 

  18. Beta Thalassemia Major

It detects 22 diseases

Price: $ 1,500 MXN


  1. Congenital hypothyroidism

  2. Hyperthyrotropinemia

  3. Phenylketonuria (PKU)- phenylalanine hydroxylase deficiency

  4. Biopterin I deficiency phenycheltonuria (GTPDH)

  5. Phenyceltonuria due to Biopterin II deficiency (DHPR)

  6. Phenyceltonuria due to Biopterin III deficiency (PAH)

  7. Phenyceltonuria due to Biopterin IV deficiency (PCD)

  8. Neonatal transient tyrosinemia

  9. Tyrosinemia type I (hepatorenal)

  10. Tyrosinemia type II (oculocutaneous)

  11. Tyrosinemia type III (Hawkasinuria 4HPPD)

  12. Argininemia

  13. Nonketotic hyperglycinemia

  14. Orian disease with classic maple syrup odor

  15. Orian disease with intermediate maple syrup odor

  16. Argininosuccinic acidemia

  17. Atroa girata

  18. Citrullinemia due to argininosuccinate synthetase deficiency

  19. Citrullinemia due to citrine deficiency

  20. HHH syndrome

  21. Homocystinuria

  22. Neonatal hypermethioninemia

It detects 28 Diseases

Price: $ 1,600 MXN


  1. Congenital hypothyroidism

  2. hyperthyrotropinemia

  3. congenital adrenal hyperplasia  salt losing variety

  4. Simple virilizing congenital adrenal hyperplasia

  5. Cystic fibrosis

  6. Hemoglobin S/C disease

  7. Hemoglobin S disease with alpha thalaemia trait

  8. disease  sickle cell beta thalassemia

  9. Hemoglonbin C disease with beta thalassemia

  10. Hemoglonbin E disease with betatalasemi

  11.   Classic galactosemia (galactose 1-phosphate uridyltransferase deficiency)

  12. Galactose variant Duarte

  13. Tyrosinemia type I (hepatorenal)

  14. Citrullinemia due to argininosuccinate synthetase deficiency

  15. Homocystinuria

  16.   Classic maple syrup urine disease

  17.   Glutaric acidemia I

  18.   SCAD (short-chain acyl-CoA dehydrogenase) deficiency

  19.   MCAD (medium-chain acyl-CoA dehydrogenase) deficiency

  20. 3-methylcrotonylglycinemia

  21. Isobutyric acidemia

  22. Propionic acidemia

  23. isovaleric acidemia

  24. Mut methylmalonic acidemia

  25. Biotinidase deficiency

  26. malonic acidemia

  27. 2-methyl-3-hydroxybutyric acidemia

  28. Avidemia 3-hydroxy-3-methylglutaric acid


It detects 76 Diseases

Price: $ 3,100 MXN

  1. Carnitine/Acylcarnitine Translocase Deficiency

  2. Carnitine Palmitoyl Transderase Deficiency Type I (CPT-1)

  3. 2,4-Dienoyl-CoA Reductase deficiency

  4. Long-chain 3-Hydroxy Acyl-CoA dehydrogenase deficiency (LCHAD)

  5. Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

  6. Multiple Acyl-CoA Dehydrogenase Deficiency (MADD or Glutaric Acidemia-Type II)

  7. Neonatal Carnitine Palmotoyl Transferase Deficiency Type I (CPT-II)

  8. Short Chain Acetyl CA Dehydrogenase Deficiency (SCAD)

  9. Short Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency (SCHAD)

  10. Trifunctional Protein Deficiency (TFP Deficiency)

  11. Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)

  12. 3-Hydroxy-3-Methylglutaryl-CoA lyase (HMG) deficiency

  13. Isobutyryl-CoA dehydrogenase deficiency

  14. Isovaleric Acidemia

  15. Glutaric acidemia type I (GA I)

  16. 2-Methylbutyryl-CoA dehydrogenase deficiency

  17. 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC Deficiency)

  18. 3-Methylglutaconyl-CoA hydratase deficiency

  19. Methylmalonic Acidemia

  20. Mitochondrial Acetoacetyl-CoA Thiolase Deficiency (3-Ketothiolase Deficiency)

  21. Propionic Acidemia (PA)

  22. Malonic Aciduria

  23. Multiple CoA Carboxylase Deficiency

  24. Medium Chain Triglyceride (MCT) Oil Administration

  25. Carnitine absorption deficiency

  26. Agyninemia

  27. Arginosuccinic Aciduria

  28. Carbamolphosphate synthetase deficiency

  29. Citrullinemia (ASA Synthetase Deficiency)

  30. Homocystinuria

  31. hypermethioninemia

  32. hyperammonemia

  33. Hyperornithinemia

  34. Homocitrullinemia (HHH Syndrome)

  35. Hyperornithinemia with Atrophy of the Circumvolutions

  36. Maple Syrup Disease

  37. 5-oxoprolinuria (Pyroglutamic Aciduria)

  38. Phenylketonuria

  39. Tyrosinemia

  40. Liver disease

  41. overeating

  42. Congenital Adrenal Hyperplasia

  43. 17-Alphahydroxyprogesterone

  44. Cystic fibrosis

  45. immunoreactive trypsinogen

  46. Congenital hypothyroidism

  47. Thyroid Stimulating Hormone (TSH)

  48. Hemoglobinopathies

  49. Sickle Cell and Other Hemoglobinopathies

  50. Galactosemia

  51. Uridyltransferase

  52. Total Galactose

  53. Immunodeficiency syndrome

  54. Severe Combined (SCID)

  55. TREC trials

  56. Gaucher disease

  57. Beta-glucocerebrosidase (ABG) deficiency

  58. Niemann-Pick disease (A/B)

  59. Acid Sphingomyelinase Deficiency (ASM)

  60. Pompe disease

  61. Lysosomal Alpha-Glucosidase Deficiency (GAA)

  62. Krabbe's disease

  63. Galactocerebrosidase deficiency (GALC)

  64. Fabry disease

  65. Alpha-Galactosidase (GLA) deficiency

  66. Hurler's disease (MPS-I)

  67. Alpha-Iduronidase deficiency (IDUA)

  68. Acylcarnitines Profile

  69. Amino Acid Profile

  70. DNA analysis for G6FD deficiency

  71. Glucose-6-Phosphate Dehydrogenase Deficiency

  72. Congenital Adrenal Hyperplasia




Simple and quick test, which detects hearing loss in newborns, without causing any pain or discomfort.

The ideal time to take this test is at birth and up to 3 months. If it is detected in this period of time, there are methods that can reduce limitations in the child’s integral development, mainly in language and learning.




The cardiological screening is a non-invasive test that helps identify critical congenital alterations of the heart, it is performed within the first 24 and 48 hours of life. It is a simple, safe, and reliable test that measures oxygen saturation in a newborn’s hand and foot.

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