What is Congenital Liver and Pancreatic Disorders in Infants?

Congenital liver and pancreatic disorders are conditions present at birth that affect the structure or function of the liver or pancreas. These may include biliary atresia, cystic fibrosis, or genetic enzyme deficiencies. Symptoms often include jaundice, poor feeding, vomiting, abdominal swelling, or failure to thrive. These disorders may cause repeated abdominal pain or digestion-related problems in infants and require early medical intervention.

How We Cure It

 Treatment varies based on the specific disorder. Some conditions like biliary atresia may require surgery (e.g., Kasai procedure), while others like enzyme deficiencies might be managed with lifelong medications or dietary modifications. In severe cases, liver or pancreatic transplant may be necessary. Early diagnosis through newborn screening and imaging helps guide treatment. Long-term follow-up is crucial for monitoring growth and development.