Timely and specific. The only comprehensive and clinically validated NIPT for autosomal recessive disorders
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Non-Invasive Prenatal Testing (NIPT) is a blood test taken from pregnant woman that uses cutting edge DNA sequencing technology to evaluate whether a baby has a high chance of a certain pathological conditions. Current NIPT can screen only for partial duplications and deletions and aneuploidy status for all autosomes, sex chromosome abnormalities, and common chromosomal conditions including trisomy 21, trisomy 18, and trisomy 13. Genome-wide screenings provide partial duplications and deletions for all autosomes and aneuploidy status for all chromosomes.
Shomool LLC is a company that carries out prenatal genetic testing services. We offer the 1st comprehensive Non-Invasive Prenatal Testing (NIPT) for Autosomal Recessive Disorders (ARD) to help evaluate whether a baby may likely be vulnerable to certain ARD. To have an autosomal recessive disorder, you inherit two changed genes (mutations), one from each parent. Examples of autosomal recessive disorders include cystic fibrosis, sickle cell anemia, and Tay-Sachs disease.
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We are the only NIPT for wide range of autosomal recessive disorders in the market, helping you protect your baby’s health.
Requiring only a single blood draw, the Shomool test offers a convenient way to get your infant screened for autosomal recessive disorders.
In addition to the common autosomal disorders, we can personalize the test according to your need with high accuracy to guide to next steps.
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