Carrier Screening

At Labassure, we are committed to helping individuals and couples make informed reproductive decisions with confidence. Carrier Screening is a vital genetic test that identifies whether an individual carries gene variants associated with inherited disorders—many of which may not present symptoms in carriers but can pose significant health risks to future offspring.

Performed through a simple blood draw, Carrier Screening analyzes specific genes to detect recessive and X-linked conditions such as thalassemia, cystic fibrosis, spinal muscular atrophy (SMA), and others. It is ideally conducted preconception or in early pregnancy, allowing couples to understand their reproductive risks and explore options if both partners are found to be carriers of the same condition.

Key Benefits:
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Proactive Family Planning: Identifies hidden risks before conception or early in pregnancy.
Simple Testing: Requires only a blood sample—no special preparation or procedures.
Broad Coverage: Screens for a wide range of severe inherited conditions.
Customizable Panels: Based on ethnicity, family history, or clinical guidelines.
Guided Genetic Counseling: Available to help interpret results and discuss next steps.

Recommended For:
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Couples planning a pregnancy
Individuals with a family history of genetic disorders
Consanguineous partners
Pregnant women during early prenatal care
Patients undergoing IVF or ICSI
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Carrier Screening at Labassure empowers families with early, actionable knowledge—supporting informed choices and peace of mind throughout the reproductive journey.

Carrier Screening

Corporate

Test & Services

Carrier Screening

Whole Exome Sequencing - WES (Single)

Corporate

Test & Services