Literature DB >> 28343205

[Biliary atresia - signs and symptoms, diagnosis, clinical management].

Ewa Orłowska1, Piotr Czubkowski1, Piotr Socha1.   

Abstract

Biliary atresia is a chronic cholangiopathy leading to progressive fibrosis of both intra- and extrahepatic bile ducts. The cause of the condition is unknown. Fundamental management of biliary atresia is surgical intervention and the outcomes of the treatment depend on the child's age with best results when performed within the first 2 months of life. Thus, the main role of pediatric healthcare is an urgent differential diagnosis and prompt qualification for the surgery, optimal postoperative management and early qualification for the liver transplantation in patients with persistent cholestasis. The authors discuss the clinical presentation, diagnosis and management of biliary atresia.

Entities:  

Keywords:  Kasai procedure; children ; cholestasis

Mesh:

Year:  2017        PMID: 28343205

Source DB:  PubMed          Journal:  Wiad Lek        ISSN: 0043-5147


  2 in total

1.  Single nucleotide polymorphisms within Adducin 3 and Adducin 3 antisense RNA1 genes are associated with biliary atresia in Thai infants.

Authors:  Wison Laochareonsuk; Piyawan Chiengkriwate; Surasak Sangkhathat
Journal:  Pediatr Surg Int       Date:  2018-03-05       Impact factor: 1.827

2.  Impact of EFEMP1 on the survival outcome of biliary atresia in Thai infants.

Authors:  Wison Laochareonsuk; Kanita Kayasut; Komwit Surachat; Piyawan Chiengkriwate; Surasak Sangkhathat
Journal:  Sci Rep       Date:  2022-09-16       Impact factor: 4.996

  2 in total

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