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Plastic and reconstructive surgery

Jacob's new jaw

Jacob’s new jaw

As a newborn, Jacob couldn't eat or breathe independently, but now he can thanks to Children's Memorial's pioneering surgery.

Jacob Bateman was just a newborn when doctors diagnosed him with Pierre Robin syndrome — a genetic disorder characterized by a cleft palate and an extremely small lower jaw, which causes difficulty in eating and breathing independently. It also poses a constant risk that the child's airway will be obstructed by the tongue falling backwards into the throat. Jacob's breathing and eating difficulties forced him to be hospitalized several times while still a newborn.

When he was able to leave the hospital, he was sent home with different monitors, oxygen and suction machines. “We were constantly worried about him catching a cold or getting congested, which would have led to more complications,” says Jacob's mother, Kristin Bateman. “It was a very difficult way to live.”

Doctors suggested that Jacob might need a surgery called a tracheostomy, which has been the only solution that would enable a child with this condition to breathe but could cause a new set of complications for the boy. Searching for a better answer, the Batemans brought Jacob to Children's Memorial.

Jacob as a baby

As a newborn, Jacob had a very small chin, one of the characteristics of Pierre Robin syndrome.

Lauren Holinger, MD, head of the Division of Otolaryngology suggested that Jacob might be a candidate for a surgical procedure that would eliminate the need for a tracheostomy. At the recommendation of pediatric plastic surgeon Pravin K. Patel, MD , Jacob became one of the youngest patients to undergo mandibular distraction osteogenesis. Surgeons implanted a device into his jaw to help lengthen bone and attached muscle, thus allowing him to breathe on his own. Currently, Children's Memorial is one of only a few hospitals in the country offering this procedure for newborns. “It is a magical process,” said Patel. “Bone is created from thin air using the body's own chemistry.”

smiling boy with a normal appearing chin After surgery, which lengthened bone and attached muscle, Jacob can breathe on his own and also has a wonderful smile!

Several weeks later, the device was removed. Soon after, Jacob was discharged and sent home without monitors or machines. Jacob is now an energetic one-year-old who keeps his parents busy!

Children's Memorial Hospital seeks philanthropic funding to enhance its programs and services. As a proud partner of the Children's Miracle Network (CMN), all funds raised in the Chicago area through CMN also benefit Children's Memorial. To find out how your support can help the hospital better serve children and families, please contact the Children's Memorial Foundation at 773.880.4237 or Foundation@childrensmemorial.org.



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