Biliary Atresia and Alpha-1 Antitrypsin Deficiency: Elliott’s Story
After being diagnosed and treated for a genetic disorder, Elliott’s troubling GI symptoms continued – leading CHOP doctors to discover he also had biliary atresia.
Hepatologists and gastroenterologists with special expertise in liver disease work with our multidisciplinary team of professionals to provide the best care for your child.
After being diagnosed and treated for a genetic disorder, Elliott’s troubling GI symptoms continued – leading CHOP doctors to discover he also had biliary atresia.
As a baby, Josie received a liver transplant. This began a 10-year journey that included bonding with her donor’s family and a generous gift to help future transplant patients.
As COVID-19 swept through Philadelphia, Briana’s biliary atresia worsened. She needed a liver transplant. CHOP safely performed the surgery. Now Briana’s future is bright.
After a liver transplant at Children’s Hospital of Philadelphia with his father as the donor, Alejandro is an active and energetic 5-year-old.
When Mya was an infant, her parents, Lissa and Jeff, learned she had biliary atresia and would eventually need a liver transplant. Here, Lissa shares the story of her daughter’s journey to a transplant at CHOP.
Born with ornithine transcarbamylase (OTC) deficiency, a rare metabolic disorder, Carter was 9 months old when he received a life-saving liver transplant at CHOP.
Chris has come a long way in the past year since he was diagnosed with biliary atresia, a liver disease. He has been helped by the Biliary Atresia Program at Children's Hospital of Philadelphia (CHOP).