How is the inpatient process for a 7-month-old boy with biliary atresia who undergoes a living donor liver transplantation at Beijing Friendship Hospital?
Neonatal biliary atresia has the potential to be cured through surgical treatment.
System ultrasound has its limitations in diagnosing congenital biliary atresia, especially in the neonatal period.
What is congenital biliary atresia? What are the symptoms? How long can a child survive without surgery?
My child was just born, but recently I noticed the child’s face was yellow and they seemed lackluster. After checking, it turned out to be biliary atresia. What are the causes of biliary atresia?
Congenital biliary atresia is one of the most important diseases in pediatric surgery, and it is also the most common indication for pediatric liver transplantation. According to clinical treatment needs, biliary atresia is classified into three types: common bile duct atresia, hepatic bile duct atresia, and portal atresia.
Understanding the symptoms of neonatal biliary atresia, including hyperbilirubinemia, clay-colored stools, and liver enlargement.
Neonatal jaundice is one of the most common conditions in newborns. This article will introduce its causes, diagnosis, and treatment methods.
Treatment Options and Long-Term Prognosis for Congenital Biliary Atresia
Does the severity of biliary atresia differ in children? What precautions should be taken in daily life?
