Condition
Pediatric Omphalocele
What You Need to Know
An omphalocele is a birth defect, which is an abnormality that occurs before birth as a fetus is forming in its mother's uterus. Some of the abdominal organs protrude through an opening in the abdominal muscles in the area of the umbilical cord. A translucent membrane covers the protruding organs.
Key Symptoms
Omphalocele is characterized by a portion of the intestines or abdominal organs protruding outside the abdominal cavity depending on the size.
Diagnosis
Your provider may spot abdominal protrusions during your ultrasound in the second or third trimester of pregnancy. Other tests to help diagnosis your baby are:
- Fetal echocardiogram
- X-ray
Treatment
Depending on the size of the omphalocele will determine the treatment plan. Treatment could include:
- Surgery
- Use of a breathing machine (mechanical ventilator)
Schedule an Appointment
Our pediatric specialists provide personalized care for your child’s physical, mental and emotional health needs. Meet the providers who treat omphalocele and schedule an appointment today.
Nick's Story
When Nick Cornelius passed his pediatrician's two-year-old well-child check-up with flying colors, his parents were thrilled. Probably even more thrilled than typical first-time toddler parents, because Nick's life up to that point had been anything but typical.
Departments that Treat Omphalocele
Rare Disease Institute - Genetics and Metabolism
Children's National Rare Disease Institute (CNRDI) is a first-of-its-kind center focused exclusively on advancing the care and treatment of children and adults with rare genetic diseases.
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