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Dergiler / Göztepe Tıp Dergisi / 2008 / Cilt: 23 - Sayı: 3

Hepatobilier yetmezlikli-transplantasyon adayı neonatal olgular ve anestezi

Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases)

Verda TOPRAK
Tezcan Gönül KELEŞ
Tülin ÖZTÜRK
Selçuk BULUT
Sayfa
95–99
Yayın Tarihi
2022-10-17
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000.
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Temel Bulgular & Veri:Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life.
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Sonuç & Katkı:Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000. Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life. Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.

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Bu Makaleye Atıf Yap

TOPRAK, V., KELEŞ, T. G., ÖZTÜRK, T., BULUT, S. (2022). Hepatobilier yetmezlikli-transplantasyon adayı neonatal olgular ve anestezi. Göztepe Tıp Dergisi, Cilt: 23 - Sayı: 3, 95–99. https://ajindex.com/articles/526272

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Kaynakça (9)

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  3. Sokol RJ, Mack C, Narkewicz MR, et al: Pathogenesis and outcome of biliary atresia: current concepts. J Pediatr Gastroenterol Nutr 2003;37:4-21
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  9. Perlmutter DH, Shepherd RW: Extrahepatic biliary atresia: a disease or a phenotype? Hepatology 2002;35:1297-1304.