Through PRENITA, Bioserve offers a range of prenatal and post-natal screening tests that provide accurate results with actionable insights, which help the clinician to analyze and provide the best outcome to the patients. PRENITA provides the most advanced Preimplantation Genetic Screening/Diagnosis (PGS/PGD), Non-Invasive Prenatal Screening Test (NIPT), Invasive Diagnostic testing… Read more
Carrier Screening

Assurance on a safe future

Carrier screening is testing an asymptomatic individual for a Genetic Disorder to understand whether they are at risk of having an affected child. Carrier screening provides the prospective parents insight about the health of their child and helps them to plan accordingly. Based on individual case studies, PRENITA Carrier Screening helps parents to identify the Genetic Conditions by opting for the appropriate tests like Next Generation Sequencing, Multiplex Ligation Probe Amplification (MLPA) or Sanger Sequencing.

Who should be offered Carrier Screening? 

  • Couples who are expecting a child or are planning a pregnancy
  • Couples with a family history of a genetic disorder
  • One of the partners is affected by a genetic disorder
  • Consanguineous Couples 
  • Couples belong to a high-risk ethnic group for specific disorders
  • Couples with an affected child for a genetic disorder or with congenital anomalies

Few of the commonly tested Genetic Disorders in India

  • Beta Thalassemia
  • Sickle Cell Anaemia    
  • Cystic Fibrosis
  • Congenital Adrenal Hyperplasia
  • Spinal Muscular Atrophy
  • Duchenne Muscular Dystrophy
  • Haemophilia A/B
  • G6PD Deficiency

 

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