The Center for Fetal Diagnosis and Treatment at The Children's Hospital of Philadelphia is an internationally recognized leader in fetal surgery and fetal care. We offer highly specialized care to mothers carrying a fetus with a known birth defect that requires treatment before or after birth. We are also home to the Garbose Family Special Delivery Unit, the world's first birthing unit for expectant parents of babies with a known birth defect.
We met Griff before he was even born! He was diagnosed with spina bifida, underwent fetal surgery in our Center at 28 weeks' gestation, and was born at his hospital back home in Minneapolis five weeks later. His family created a video to document how great he is doing today - be sure to watch!
Look at Amelia now!
Look at Lilliana now!
Look at Loxley now!
Join us in wishing a very happy belated birthday to Marley!
We are excited to announce the teen patient reunion is back again this year as part of our annual Fetal Family Reunion on June 2! From noon to 2 p.m., we'll have special activities for former patients ages 12 and older. This is a great chance to meet and have fun with other youth who have had unique experiences at CHOP. Follow the link for information on how to register.
A new study from Dr. William Peranteau, our Center for Fetal Research and colleagues at Penn Medicine was published today in Science Translational Medicine! This proof-of-concept study showed that, one day, in-utero gene editing could be a promising new approach for treating lung diseases before birth.
Today, Peyton is in fifth grade, just celebrated her 11th birthday, and loves running track - an impressive feat considering Peyton was born with a congenital diaphragmatic hernia, when the diaphragm muscle fails to close during prenatal development, and the contents from the abdomen migrate into the baby's chest. At four days old, she underwent surgery. Since then, she and her family have made it their mission to help other families who were given the same scary diagnosis. Read for her full story. #CDHAwarenessMonth #ForBreakthroughs
Molly is registered for our upcoming Family Reunion! Are you?
"I didn't want to hear it was OK, and not to worry. I liked how serious CHOP was about the condition," recalls Meredith. When she and her husband Jeff learned their unborn baby had a sacrococcygeal teratoma (SCT), they traveled from their home in New Jersey and came to our Center for treatment. This is Rowan's story.
El and Matt were thrilled when they learned they were expecting their first child. But at their 20-week ultrasound, they received devastating news: their baby had a sacrococcygeal teratoma (SCT) — a large tumor located at the base of the tailbone. This is their story.
We ❤️ Wawa and our volunteers! From all of us at CHOP, Happy #WawaDay and National Volunteer Week!