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Chromosomal Studies – Amniotic Fluid Karyotype is a prenatal diagnostic test that analyzes fetal chromosomes using a sample of amniotic fluid. It detects chromosomal abnormalities such as Down syndrome, trisomy 18, and structural rearrangements.
Sample Type : Amiotic Fluid
Methodology : Conventional Cytogenetics: Culture + Chromosome analysis
TAT : 30 Days
The **SPINAL MUSCULAR ATROPHY (SMA) Test** is a cutting-edge genetic screening tool designed to detect mutations in the **SMN1 gene**, the primary cause of SMA, a severe neuromuscular disorder. This highly accurate test enables **early diagnosis**, allowing for timely medical intervention and personalized treatment plans. It is **non-invasive**, requiring only a simple blood or saliva sample, and delivers **fast, reliable results**. Ideal for **newborn screening, carrier detection, and prenatal testing**, it empowers individuals and families with crucial genetic insights. With advanced technology ensuring **high sensitivity and specificity**, this test is a must-have for proactive healthcare and informed decision-making.