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Newborn Screening

About Newborn Screening

Newborn screening is a preventive healthcare program designed to detect serious genetic, metabolic, hormon...

Overview

Early identification of these conditions allows immediate treatment before symptoms develop, preventing severe disability, developmental delay, or life-threatening complications.

Understanding The Procedure

Symptoms That May Require Newborn Screening

  • Need for preventive newborn evaluation
  • Family history of genetic disorders
  • Premature birth
  • High-risk pregnancy history
  • Suspicion of congenital abnormalities

Recovery & Outlook

Screening is performed shortly after birth

Abnormal findings are evaluated quickly

Repeat testing may be required when necessary

Early treatment begins after diagnosis

Long-term monitoring improves developmental outcomes

Risks

  • False-positive screening results
  • Anxiety regarding abnormal findings
  • Need for repeat testing
  • Delayed treatment if screening missed
  • Minor discomfort during sample collection

Post-Operative Care

  • Attend newborn follow-up appointments
  • Repeat tests if recommended
  • Follow treatment plans promptly
  • Maintain regular pediatric evaluations
  • Monitor developmental milestones carefully

Conclusion

Newborn screening supports early diagnosis and prevention of severe childhood complications.

Doctors Who Perform Newborn Screening

Meet experienced paediatrics (child-care) doctors who regularly evaluate and perform newborn screening.

Dr Keshava Murthy M

Dr Keshava Murthy M

MBBS,MS,MRCS,MCH(Pediatric Surgery)

KMC: 59978

Consultant Pediatric Surgeon

Seema G

Seema G

MBBS, MD

KMC: 124478

Consultant Pediatrician and Neonatologist

Dr Mohamed Rufaiqa

Dr Mohamed Rufaiqa

MBBS, DCH (DNB)

KMC: TMN 0000336 KTK

Consultant Paediatrician

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