A baby girl with Alagille syndrome and related liver problems that were not responding to standard medication was also diagnosed with a rare liver…
Biliary atresia is a rare liver disease affecting infants, in which the ducts that carry the digestive fluid bile from the liver to the small intestine are blocked.
The first-line treatment for biliary atresia, a disorder in which certain bile ducts outside the liver are blocked or absent, typically is a surgical procedure called a Kasai portoenterostomy, which aims to restore the normal flow of bile in the patient’s body.
ALAGILLE SYNDROME
NewsA baby girl with Alagille syndrome and related liver problems that were not responding to standard medication was also diagnosed with a rare liver…
A global clinical trial testing Mirum Pharmaceuticals’ oral therapy maralixibat in people with itching, or pruritus, due to rare cholestatic conditions has finished…
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