BabyMap Genetic Carrier Screening Cost (Single) | Mapmygenome

Genomepatri Whole Exome Sequencing - Mapmygenome
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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.

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30000

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Reviews & Comments

★★★★★
★★★★★

Vijay M

excellent product. turn around time was quick and report easy to understand. good investment

Raman

My parents were even more excited than both of us to get this done. There is a history of consanguinity in our family so it was imperative for us to do it. My doctor also strongly recommended that we do a carrier screen. She was aware of the test that Mapmygenome did and directed us there.
The process was smooth and the team is exceptional. The report came back in less than 10 days.

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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: http://mapmygenome.in/blog/babymap-carrier-screening-india-adw

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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