Journals / Zeynep Kamil Tıp Bülteni / 2016 / Cilt: 47 - Sayı: 4

A Newborn Presented with Cholestasis and Diagnosed with Congenital Pituitary Hormone Deficiency

Neonatal Kolestaz ile Başvuran Konjenital Hipofiz Hormon Eksikliği Tanılı Yenidoğan Olgusu

Pages
83–85
DOI
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AI Summary & Key Takeaways

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

An infrequent reason of neonatal cholestasis is congenital pituitary hormone deficiency

📌 3 Key Takeaways

🎯
Objective & Hypothesis:An infrequent reason of neonatal cholestasis is congenital pituitary hormone deficiency
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Key Findings & Data:An infrequent reason of neonatal cholestasis is congenital pituitary hormone deficiency
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Conclusion & Impact:An infrequent reason of neonatal cholestasis is congenital pituitary hormone deficiency
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

An infrequent reason of neonatal cholestasis is congenital pituitary hormone deficiency

Özet

Konjenital hipofiz hormon eksikliği neonatal kolestazın sık olmayan nedenidir. Yenidoğan döneminde klinik bulguları kolestaz ve hipoglisemidir. Sezeryan ile, 37 haftalık, 3700 gr doğan kız bebekte postnatal birinci hafta hipoglisemi, 3. haftada kolestaz bulguları gelişti. Çoklu hipofiz hormon eksikliği saptandı. Büyüme hormonu tedavisi ile kolestaz bulguları düzeldi. Konjenital hipofiz hormon eksikliği, hipoglisemi ve kolestazı olan yenidoğanlarda ayırıcı tanıda akılda tutulmalıdır

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Cite This Article

ÖZALKAYA, E., AKDAĞ, A., PAPATYA, E. D., TOPÇUOĞLU, S. (2016). A Newborn Presented with Cholestasis and Diagnosed with Congenital Pituitary Hormone Deficiency. Zeynep Kamil Tıp Bülteni, Cilt: 47 - Sayı: 4, 83–85. https://ajindex.com/articles/335236

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