Скачать или смотреть Detecting Genetic Disorders Early: Complete Guide to NT Scan & Double Marker Test 💛

Many expecting moms feel anxious when they hear about genetic tests…
“Is my baby okay?”
“Are these tests safe?”
Let’s understand this clearly and calmly. 🌸

Early screening tests like NT Scan and Double Marker Test help detect the risk of certain genetic conditions—so timely care and reassurance are possible.

💛 What Is an NT Scan?
👉 NT (Nuchal Translucency) scan is a special ultrasound
👉 Measures fluid behind the baby’s neck
👉 Done between 11–13 weeks of pregnancy
👉 Increased thickness may indicate risk of genetic disorders
👉 Completely safe for both mother and baby

💛 What Is the Double Marker Test?
A simple blood test done for the mother.
👉 Measures two pregnancy-related hormones
👉 Helps assess risk for conditions like:
• Down syndrome
• Trisomy 18
• Trisomy 13
👉 Usually done along with NT scan for better accuracy

💛 Why Are These Tests Important?
👉 Detects genetic risk early in pregnancy
👉 Helps doctors plan next steps if needed
👉 Reduces anxiety with timely reassurance
👉 Supports informed decision-making for parents

💛 Important to Remember
👉 These are screening tests, not diagnostic tests
👉 “High risk” does NOT mean baby has a problem
👉 Further tests may be advised only if required
👉 Most reports come back normal 💛

Early screening is not about fear…
It’s about care, clarity, and confidence for you and your baby 🌸

👩‍⚕️ Dr. Niharika Allu, MS(OBG), DNB, FICOG
Consultant Obstetrician & Gynecologist
Rainbow Children’s Hospital, Visakhapatnam
Specialist in high-risk pregnancy, prenatal screening & women’s health

#NTScan #DoubleMarkerTest #GeneticScreening #PregnancyCare #FirstTrimester #HealthyPregnancy #HighRiskPregnancy #DrNiharikaAllu