Pediatric surgeon in Bangalore

Meet Our Lead Pediatric Surgeon in Bangalore

Dr. Antony Robert Charles

Director & Chief Consultant, Pediatric Surgery
Pediatric surgeon in Bangalore
Director & Chief Consultant, Pediatric Surgery

Dr. Antony Robert Charles is the Director & Chief Consultant at KinderSurge, Bengaluru, and a highly respected pediatric surgeon and pediatric urologist with over 25 years of experience. He specialises in pediatric laparoscopy, urological reconstructive surgeries, and neonatal surgical emergencies, delivering advanced, child-focused surgical care.

Internationally trained and deeply committed to ethical medical practice, Dr. Robert is known for combining clinical excellence with compassion. Beyond surgery, he is a TEDx speaker, medical ethicist, and the founder of the ChildFirst Foundation, working to ensure humane, ethical, and world-class healthcare for children.

Dr. Antony Robert Charles – Experienced Best Pediatric Surgeon in Bangalore providing expert surgical care for newborns, children, and adolescents with a compassionate, child-focused approach.

+
Years of Experience
+
Successful Surgeries
+
Children Treated
Languages Spoken
+
Years of Experience
+
Successful Surgeries
+
Children Treated
Languages Spoken

Congenital Anomaly & Birth Defect Surgery in Bangalore — Expert Neonatal Surgical Care for Your Baby

Hearing that your newborn needs surgery is one of the most frightening moments a parent can face. You have questions. You need answers — fast. Dr Antony Robert Charles, a trusted senior pediatric and neonatal surgeon in Bangalore, provides expert, compassionate surgical care for babies born with congenital anomalies and structural birth defects. From esophageal atresia to Hirschsprung disease, his team is equipped and ready — day or night.

Congenital anomaly surgery in Bangalore corrects structural birth defects in newborns and infants — including esophageal atresia, intestinal atresia, tracheoesophageal fistula, anorectal malformations, and Hirschsprung disease. Dr Antony Robert Charles is a specialist pediatric surgeon in Bangalore offering advanced neonatal surgical care with high success rates.

What Are Congenital Anomalies?

A congenital anomaly — also called a birth defect or congenital malformation — is a structural problem that develops in a baby’s organs or body parts while still in the womb. Some are diagnosed on antenatal ultrasound before birth. Others become apparent in the first hours or days of life.

These conditions are not caused by anything you did or didn’t do as a parent. Most birth defects occur due to complex genetic, environmental, or developmental factors during fetal development.

Common surgically correctable congenital anomalies include:

  • Esophageal Atresia (EA) — the food pipe (esophagus) is incomplete or missing a section
  • Tracheoesophageal Fistula (TEF) — an abnormal connection between the windpipe and food pipe
  • Intestinal Atresia — a blockage or gap in the small or large intestine
  • Anorectal Malformation (ARM) — the anus or rectum is absent or incorrectly formed
  • Hirschsprung Disease — missing nerve cells in part of the large intestine causing obstruction
  • Duodenal Atresia — blockage of the first section of the small intestine
  • Malrotation & Volvulus — the intestines are abnormally rotated, risking twisting and blood loss
  • Congenital Diaphragmatic Hernia (CDH) — abdominal organs herniate into the chest cavity
  • Biliary Atresia — blocked bile ducts in the liver

Warning Signs: When to Seek Emergency Help Immediately

EMERGENCY WARNING SIGNS — Take your baby to the nearest hospital NOW if you notice:

  • Baby cannot swallow or is choking, coughing, or turning blue during every feed
  • Green or yellow (bilious) vomiting in a newborn
  • No passage of first stool (meconium) within 24–48 hours of birth
  • Severely swollen or rigid abdomen
  • Absence of a normal anal opening
  • Baby is in obvious pain, inconsolably crying, or extremely lethargic
  • Rapid breathing with a sunken chest or pulled-in neck muscles
  • Any sign of jaundice deepening rapidly after the first week

These are potentially life-threatening conditions requiring immediate neonatal surgical evaluation. Do not wait. Call Dr Antony Robert Charles’s emergency line or proceed to the nearest pediatric surgical facility in Bangalore.

Symptoms by Condition

Esophageal Atresia & Tracheoesophageal Fistula (EA/TEF) Symptoms

  • Excessive drooling or foamy bubbles at the mouth from birth
  • Choking, gagging, or coughing with every feed
  • Breathing distress (fast breathing, blue lips)
  • Inability to pass a feeding tube into the stomach
  • Often diagnosed on antenatal ultrasound (polyhydramnios)

Intestinal Atresia Symptoms in Newborns

  • Bilious (green) vomiting within first 24–48 hours
  • Abdominal distension (bloating)
  • Failure to pass meconium
  • Prenatal finding of “double bubble” sign on ultrasound (duodenal atresia)

Anorectal Malformation (Imperforate Anus) Symptoms

  • No visible anal opening at birth
  • Routine newborn exam typically identifies this at delivery
  • Meconium passed from an abnormal location (urethra, vagina, perineum)
  • Abdominal distension if untreated

Hirschsprung Disease Symptoms

  • Delayed passage of meconium (more than 48 hours after birth)
  • Chronic constipation beginning in infancy
  • Abdominal distension and vomiting
  • Explosive release of gas and stool after rectal examination
  • Poor weight gain and feeding difficulties

Congenital Diaphragmatic Hernia (CDH) Symptoms

  • Severe breathing difficulty immediately after birth
  • Breath sounds absent on one side of chest
  • Scaphoid (sunken) abdomen
  • Usually diagnosed prenatally on ultrasound

Causes & Risk Factors

Most congenital anomalies arise from a combination of genetic and environmental factors during the first trimester — when organ systems are forming. In the majority of cases, parents have done nothing wrong.

Known contributing factors include:

  • Genetic mutations or chromosomal abnormalities (e.g., Down syndrome is associated with duodenal atresia)
  • Folic acid deficiency in early pregnancy
  • Infections during pregnancy (rubella, cytomegalovirus)
  • Certain medications or exposures during first trimester
  • Family history of specific anomalies
  • Multifactorial developmental disruptions — the most common, and largely unpredictable

Knowing the cause matters for family counseling and future pregnancies, but it does not change the love and care your baby receives today.

Diagnosis: How Are Congenital Anomalies Detected?

Before Birth (Prenatal Diagnosis)

  • Anomaly scan (18–20 weeks): Detailed fetal ultrasound detects many structural defects
  • Fetal MRI: Provides detailed images of brain, lung, and abdominal structures
  • Amniocentesis / CVS: For chromosomal analysis if genetic cause suspected
  • Polyhydramnios (excess amniotic fluid) may indicate esophageal or intestinal blockage

After Birth (Postnatal Diagnosis)

  • Clinical examination by neonatologist and pediatric surgeon at birth
  • X-ray (plain abdominal / chest): Shows gas patterns, bowel obstruction, CDH
  • Contrast studies: Barium swallow, contrast enema to outline blockages or fistulas
  • Ultrasound: Abdominal, renal, and spine assessment
  • Rectal suction biopsy: Confirms Hirschsprung disease
  • Blood tests & ECHO: Assess associated cardiac and metabolic conditions
Early, accurate diagnosis is critical. Dr Antony Robert Charles works closely with neonatologists and radiologists to ensure rapid workup and surgical planning — minimizing the time your baby spends waiting.

Diagnosis: How Are Congenital Anomalies Detected?

  • Before Birth (Prenatal Diagnosis)

    • Anomaly scan (18–20 weeks): Detailed fetal ultrasound detects many structural defects
    • Fetal MRI: Provides detailed images of brain, lung, and abdominal structures
    • Amniocentesis / CVS: For chromosomal analysis if genetic cause suspected
    • Polyhydramnios (excess amniotic fluid) may indicate esophageal or intestinal blockage

    After Birth (Postnatal Diagnosis)

    • Clinical examination by neonatologist and pediatric surgeon at birth
    • X-ray (plain abdominal / chest): Shows gas patterns, bowel obstruction, CDH
    • Contrast studies: Barium swallow, contrast enema to outline blockages or fistulas
    • Ultrasound: Abdominal, renal, and spine assessment
    • Rectal suction biopsy: Confirms Hirschsprung disease
    • Blood tests & ECHO: Assess associated cardiac and metabolic conditions
    Early, accurate diagnosis is critical. Dr Antony Robert Charles works closely with neonatologists and radiologists to ensure rapid workup and surgical planning — minimizing the time your baby spends waiting.

Treatment: Surgical Options Explained

Every baby and every anomaly is unique. Dr Antony Robert Charles creates a personalized surgical plan based on the specific condition, baby’s weight and stability, and presence of associated anomalies.

Esophageal Atresia / TEF Surgery (Bangalore)

  • Primary repair: The two ends of the esophagus are connected (anastomosed) and the fistula is closed
  • Minimally invasive thoracoscopic (keyhole) approach available for eligible babies
  • Long-gap EA may require staged repair over weeks to months
  • Performed within 24–48 hours of birth in stable infants

Intestinal Atresia Surgery

  • Resection of the atretic (blocked) segment and reconnection (anastomosis) of healthy bowel
  • Laparoscopic approach increasingly used in larger newborns
  • Temporary stoma (colostomy or ileostomy) may be needed in complex cases

Anorectal Malformation Surgery (Imperforate Anus)

  • Low anomalies: Primary perineal surgery (anoplasty) within first 48 hours
  • High anomalies: Staged repair — protective colostomy first, followed by posterior sagittal anorectoplasty (PSARP) at 3–6 months
  • Minimally invasive laparoscopic-assisted PSARP (LAARP) in selected cases

Hirschsprung Disease Surgery

  • Pull-through procedure: Diseased bowel (lacking nerve cells) is removed; healthy bowel is connected to the anus
  • Laparoscopic Soave or Swenson pull-through performed in a single stage in most cases
  • Temporary protective stoma if baby presents in enterocolitis or with significant dilation

Congenital Diaphragmatic Hernia (CDH) Surgery

  • Stabilization first — surgery after NICU optimization (often 48–72 hours)
  • Repair of the diaphragmatic defect via open or minimally invasive (thoracoscopic) approach
  • Long-term follow-up for lung growth and reflux

Malrotation & Volvulus (Ladd’s Procedure)

  • Surgical emergency if volvulus (twisting with loss of blood supply) is present
  • Ladd’s procedure: untwisting bowel, dividing Ladd’s bands, and appendectomy
  • Time-critical — delayed surgery risks loss of bowel

Recovery: What to Expect After Congenital Anomaly Surgery

Recovery timelines vary by condition and complexity, but here is what most families can expect:

Condition

ICU/Hospital Stay

Full Recovery

EA/TEF repair

2–4 weeks

3–6 months (feeding milestones)

Intestinal atresia

2–3 weeks

4–8 weeks post-discharge

Anorectal malformation (low)

3–5 days

Weeks (with dilatation program)

Hirschsprung pull-through

1–2 weeks

Months (bowel retraining)

CDH repair

4–8 weeks

Months to years (lung development)

Malrotation/Ladd’s

5–10 days

2–4 weeks

During recovery, your baby will receive:

  • NICU or PICU monitoring by a dedicated neonatal nursing team
  • IV nutrition (TPN) until feeds are established
  • Careful wound care and pain management
  • Regular review by Dr Antony Robert Charles and his team
  • Feeding support — lactation guidance and specialized feeding techniques
  • Parent education before discharge

You will never feel alone in this journey. Dr Antony’s team believes in keeping parents informed, involved, and supported at every step.

📞 Book a Consultation with Dr. Antony Robert Charles — Pediatric Urologist, Bangalore

Your child’s urinary health cannot wait. Neither should you. Whether you’re in Whitefield, Koramangala, Marathahalli, Hebbal, or Sarjapur Road — expert, compassionate pediatric urology care is available for your family.

What to Expect at Your First Visit:

✔ Thorough history and physical examination ✔ Clear explanation of your child’s condition in simple language ✔ A personalized investigation and treatment plan ✔ Honest, evidence-based advice — no unnecessary procedures ✔ Time for all your questions to be answered

📅 Appointment Options:

  • In-Person Consultation — Bangalore clinic (address on contact page)
  • Teleconsultation — Available for initial queries and follow-ups
Emergency Contact — For urgent urological concerns

Serving Families Across Bangalore — Local Expertise You Can Trust

Dr Antony Robert Charles provides specialized pediatric and neonatal surgical care to families across all major areas of Bangalore:

Congenital Anomaly Surgery Near Whitefield, Bangalore

Families in Whitefield, ITPL, Varthur, and Kadugodi can access expert neonatal surgical care without travelling to distant parts of the city. Dr Antony’s practice is easily reachable from Whitefield, and emergency consultations are available around the clock.

Birth Defect Surgery Near Marathahalli, Bangalore

Parents in Marathahalli, Doddanekundi, and Brookefield have trusted Dr Antony Robert Charles for complex neonatal surgeries requiring skilled hands and compassionate care. Quick access routes from Marathahalli make emergency presentations timely.

Pediatric Surgery Near Koramangala, Bangalore

Koramangala, HSR Layout, and BTM Layout families seeking expert congenital anomaly surgery will find Dr Antony Robert Charles to be one of Bangalore’s most experienced and accessible pediatric surgeons for neonatal conditions.

Neonatal Surgical Expertise Near Hebbal, Bangalore

Families from Hebbal, Yelahanka, Jakkur, and Thanisandra can reach Dr Antony’s facility comfortably. He routinely manages referrals from neonatal units in north Bangalore for complex birth defect surgeries.

Congenital Anomaly Surgery Near Sarjapur Road, Bangalore

Parents located along Sarjapur Road, Bellandur, Haralur, and Carmelaram can access trusted neonatal surgical expertise close to home. Dr Antony Robert Charles’s team understands the urgency that comes with a newborn surgical diagnosis.

Frequently Asked Questions:

Q1: What is congenital anomaly surgery in newborns?

Congenital anomaly surgery corrects structural birth defects present at birth — such as esophageal atresia, intestinal atresia, anorectal malformation, and Hirschsprung disease — allowing the baby's organs to function normally. These surgeries are typically performed by a specialist pediatric and neonatal surgeon within hours to days of birth.

Q2: Which is the best hospital for birth defect surgery in newborns in Bangalore?

Families across Bangalore — including areas like Whitefield, Koramangala, Marathahalli, Hebbal, and Sarjapur Road — trust Dr Antony Robert Charles for neonatal and congenital anomaly surgery. He offers advanced minimally invasive surgical techniques, dedicated NICU support, and extensive experience with complex neonatal conditions.

Q3: Is esophageal atresia surgery successful in India?

Yes. With timely diagnosis and expert surgical repair, survival rates for esophageal atresia exceed 90% in otherwise healthy newborns in experienced centers. Early detection — often on antenatal ultrasound — and prompt referral to a specialist pediatric surgeon are the most important factors in a good outcome.

Q4: What are the signs of intestinal atresia in a newborn?

Signs of intestinal atresia include failure to pass meconium (first stool) within 24–48 hours, a swollen or distended abdomen, green (bilious) vomiting, and feeding difficulties. These require immediate pediatric surgical evaluation — do not wait for a routine appointment.

Q5: How soon after birth is Hirschsprung disease surgery performed?

Hirschsprung disease surgery (pull-through procedure) is typically performed within the first few weeks to months of life, depending on the severity. If the baby presents with Hirschsprung-associated enterocolitis (HAEC) — a serious infection — emergency intervention with bowel decompression or a protective colostomy may be needed first.

Q6: Can anorectal malformation be detected before birth?

Anorectal malformation (imperforate anus) is rarely detected on routine prenatal ultrasound. It is most often identified during the routine physical examination performed immediately after birth. The absence of a normal anal opening is the key finding. Associated anomalies (spinal, renal, cardiac) are screened for systematically after diagnosis.

Q7: What is the recovery time after congenital anomaly surgery in babies?

Recovery depends on the specific condition. Most babies with intestinal atresia or anorectal malformation are ready for discharge within 2–4 weeks. Conditions like esophageal atresia or congenital diaphragmatic hernia may require a longer NICU stay of 4–8 weeks or more. Dr Antony Robert Charles provides detailed, individualized recovery guidance to each family.

Q8: Is congenital anomaly surgery available near Whitefield or Koramangala Bangalore?

Yes. Dr Antony Robert Charles provides neonatal and congenital anomaly surgical services accessible to families across Bangalore — including Whitefield, Marathahalli, Koramangala, Hebbal, and Sarjapur Road. His clinic and operating facilities are centrally located with emergency access available 24/7.

Q9: What is the cost of birth defect surgery in Bangalore?

The cost of congenital anomaly surgery in Bangalore varies depending on the type of defect, complexity of repair, duration of NICU stay, and associated care required. Dr Antony Robert Charles's team provides transparent cost estimates after initial assessment and assists families with insurance and financial planning guidance.

Q10: Can babies born with birth defects live a normal life?

Yes — the majority of babies who receive timely, expert surgical correction of congenital anomalies go on to live healthy, normal lives. Long-term outcomes depend on the specific condition, timely intervention, and quality of follow-up care. Many conditions — including intestinal atresia, anorectal malformation, and Hirschsprung disease — have excellent long-term quality-of-life outcomes with expert management.

Patient Education

Evidence-Based Insights for Parents

Pediatric Consultant

Dr. Antony Robert Charles Discusses Surgery in Children

Get more info

EMERGENCY CALL

Get a helpful insight

Read Out The Blogs

Health Tip

Little Tips for Big Health

Dr. Antony Robert Charles

4 Videos

Why Choose Dr Antony Robert Charles for Congenital Anomaly Surgery in Bangalore?

Specialist Pediatric & Neonatal Surgeon

Dr Antony Robert Charles is a highly experienced pediatric and neonatal surgeon with dedicated training and extensive operative experience in congenital anomaly surgery. He has performed hundreds of neonatal surgical procedures across the full spectrum of birth defects.

Minimally Invasive & Advanced Surgical Techniques

Where appropriate, Dr Antony utilizes laparoscopic (keyhole) and thoracoscopic approaches — resulting in smaller scars, less pain, faster recovery, and reduced risk of wound complications for your baby.

Multidisciplinary Neonatal Care

He works closely with a dedicated team of neonatologists, pediatric anesthesiologists, radiologists, cardiologists, and specialized NICU nurses — ensuring your baby receives comprehensive, coordinated care from diagnosis to discharge.

Clear, Compassionate Communication

Dr Antony Robert Charles believes parents deserve honest, plain-language explanations at every step. He makes time to explain diagnoses, surgical plans, expected outcomes, and recovery — answering every question without rush.

Accessible Across Bangalore — Including Emergencies

With facilities accessible to families from Whitefield, Marathahalli, Koramangala, Hebbal, and Sarjapur Road, Dr Antony is available for emergency consultations and urgent surgical intervention when your baby needs it most.

Trusted by Hundreds of Bangalore Families

Families across Karnataka and beyond have trusted Dr Antony Robert Charles with their most precious moments — bringing their newborns through complex surgeries and into healthy, thriving childhoods.