BabyMap NBS

BabyMap NBS
In Stock

BabyMap carrier screening provides you and your physician with information regarding your newborns risks for developing genetic conditions and provides you with recommendations to keep the conditions under check

QTY :

30000

Add to cart

Add to wishlist


Reviews & Comments

★★★★★
★★★★★

Balaji

My pediatrician told me about newborn screening and various options. Babymap seemed the most comprehensive and we wanted to make sure that our baby has the best screening possible.
The whole process was smooth and the doctor very helpful.
The only possible down side could be the price point. I wish it came down to 20,000 and then more people would get it done.

Write Review

BabyMap BabyMap Newborn Screening brings advanced genetic technology to newborn screening. Here are a few reasons why BabyMap is the perfect choice for parents who want to be proactive and give their children the very best start in life:


Why is Newborn Screening Important?



  • DNA Based: BabyMap tests DNA- the "blueprint" that codes for health or disease- for changes that could indicate a serious but preventable genetic condition.

  • Quick Results: Since DNA is typically unchanged (compared to fluctuations in levels of biochemicals) BabyMap can be performed immediately after birth. There is no need to wait for 48 hours before the baby's metabolism kicks in.

  • Coverage: BabyMap Newborn Screening tests 0ver 90 genes that are clinically linked to over 70 genetic conditions

  • Confirmatory Testing: Since BabyMap is DNA based, it does not require extensive follow-up testing or additional confirmatory testing. It is a genetic test that can be used for screening as well confirmation.


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-newborn-screening-india-adw

Call : 1800-102-4595 write to : info@mapmygenome.in
Toll Free Number 1800-102-4595 | Email info@mapmygenome.in | © 2017 Mapmygenome™ Indian Genomics Company
Selected Product breast ovary caner panel
send request