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Journals / The Journal of Pediatric Research / 2021 / Cilt: 8 - Sayı: 4

Congenital Portosystemic Shunt as a Rare Cause of Neonatal Cholestasis: Case Report

Cemil OKTAY
Sibel YAVUZ
Mehmet Emin PARLAK
Gökhan ÖZEL
Pages
502–505
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We present a case of congenital intrahepatic portosystemic venous shunt as a rare cause of neonatal cholestasis with current treatment recommendations.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Cholestatic jaundice is a complex diagnostic problem with a wide spectrum of possible differential diagnosis in early infancy.
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Key Findings & Data:Cholestatic jaundice is a complex diagnostic problem with a wide spectrum of possible differential diagnosis in early infancy.
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Conclusion & Impact:We present a case of congenital intrahepatic portosystemic venous shunt as a rare cause of neonatal cholestasis with current treatment recommendations.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Cholestatic jaundice is a complex diagnostic problem with a wide spectrum of possible differential diagnosis in early infancy. We present a case of congenital intrahepatic portosystemic venous shunt as a rare cause of neonatal cholestasis with current treatment recommendations.

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Cite This Article

OKTAY, C., YAVUZ, S., PARLAK, M. E., ÖZEL, G. (2021). Congenital Portosystemic Shunt as a Rare Cause of Neonatal Cholestasis: Case Report. The Journal of Pediatric Research, Cilt: 8 - Sayı: 4, 502–505. https://ajindex.com/articles/362710

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References (10)

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