Spinal Muscular Atrophy (SMA) Carrier Screening

Spinal Muscular Atrophy (SMA) Carrier Screening

SMA Carrier Screening is a genetic test that identifies individuals carrying mutations in the SMN1 gene, responsible for Spinal Muscular Atrophy (SMA). While carriers themselves do not develop the disease, they can pass the mutation to their children if both parents are carriers.

This test allows families to:
• Assess the risk of having a child with SMA
• Plan a healthy pregnancy and make informed reproductive decisions
• Receive timely genetic counseling if carrier status is detected

Our laboratory uses advanced molecular diagnostic methods, including sequencing and quantitative gene analysis, to accurately identify SMA carriers. Precise test results help doctors and families make responsible decisions and reduce the risk of hereditary diseases.