BabyMap Carrier (Couple)

BabyMap Couple
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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.

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60000

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Reviews & Comments

★★★★★
★★★★★

Srinivas

I moved back from the US 2 years ago. I had heard of carrier screening there. I searched for something similar in India as I was planning on getting married and found Babymap from Mapmygenome.
Both me and my potential partner did the test.
We found that I was a carrier for G6Pd but luckily he did not. so all was well and we carried on.
It was very quick and we got our reports rather quickly.

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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

Call : 1800-102-4595 write to : info@mapmygenome.in
Toll Free Number 1800-102-4595 | Email info@mapmygenome.in | © 2017 Mapmygenome™ - Know Yourself
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