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BabyMap Genetic Carrier Screening (Single)

BabyMap Carrier (Single)
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BabyMap Genetic carrier screening at low cost provides you & your physician with information regarding the reproductive risks and the impact on your future children.

This includes:
- Primary Genotype Report
- Personalised Genetic Counseling session (~45 mins)
- Recommendations and guidelines from our counselor. This may include other screening tests if any.
A physician's summary or a genetic counseling session is necessary before purchase.


$ 499

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BabyMap carrier screening provides you and your physician with information regarding your reproductive risks and how they may impact your future children. By determining each parent’s carrier status, couples planning a pregnancy can identify their chance for having a child with a genetic condition. Our genetic counselors are with you every step of the way.

Key benefits for parents-to-be and those planning a family:

  • Early detection of 71+ metabolic conditions with successful treatment options

  • Genetic counseling to understand carrier status and to chart out an informed plan for pregnancy management

Some conditions covered:

  • Organic Acid Disorders: 3-Hydroxy-3-methylglutaric aciduria (3-hydroxy-3-methylglutaryl-CoA lyase deficiency), Glutaric acidemia Type I, Methylmalonic acidemia (methymalonyl-CoA mutase deficiency), Propionic acidemia.

  • Fatty Acid Oxidation Disorder Conditions: Long chain L-3 hydroxyacyl-CoA dehydrogenase deficiency.

  • Amino Acid Disorder Conditions: Benign hyperphenylalaninemia, Homocystinuria, Hypermethioninemia, Maple syrup urine disease, Phenylketonuria, Tyrosinemia.

  • Endocrine / Hemoglobin Conditions: Congenital adrenal hyperpalsia, Primary congenital hypothyroidism, S, Beta thalassemia, Sickle cell anemia (S,S Disease), Sickle cell disease (S,C Disease).

  • Other Conditions: ADA Severe combined immunodeficiency (Adenosine deaminase), Biotinidase deficiency, Cystic fibrosis, Nonsyndromic deafness (Hearing loss), X-linked Severe combined immunodeficiency.

  • Additional BabyMap Conditions: Fabry disease (GLA deficiency), Glucose-6-Phospohate Dehydrogenase Deficiency, Mucopolysaccharidosis type 1, Niemann-Pick disease, X-linked adrenoleukodystrophy

more info:

Call : 1800-102-4595 write to :
Toll Free Number 1800-102-4595 | Email | © 2018 Mapmygenome™ - Know Yourself
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