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Journals / Meandros Medical And Dental Journal / 2004 / Cilt: 5 Sayı: 2

Crouzon Syndrome: Neonatal Case Report

Murat HIZARCIOĞLU
Pamir GÜLEZ
Ertan KAYSERİLİ
Hale YENER
Serap KORKMAZ
Pages
27–29
Publication Date
2004-08-01
DOI
—
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AI Summary & Key Takeaways

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

This case was presented due to it's importance as a rarely seen syndrome and for being diagnosed due to phenotypic characteristics features.

📌 3 Key Takeaways

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Objective & Hypothesis:Six day old girl was admitted to hospital for jaundice and abnormalities of the head, face and eyes.
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Key Findings & Data:Her physical examination showed synostosis of cranial sutures, brachycephaly, beak-like nose, exophthalmos and high arched palate.
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Conclusion & Impact:This case was presented due to it's importance as a rarely seen syndrome and for being diagnosed due to phenotypic characteristics features.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Crouzon sendromu · kraniyosinostoz · dismorfik fenotipik özellikler

Abstract

Six day old girl was admitted to hospital for jaundice and abnormalities of the head, face and eyes. Her physical examination showed synostosis of cranial sutures, brachycephaly, beak-like nose, exophthalmos and high arched palate. Crouzon syndrome was diagnosed by physical examination and imaging tecniques. This case was presented due to it's importance as a rarely seen syndrome and for being diagnosed due to phenotypic characteristics features.

Özet

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Cite This Article

HIZARCIOĞLU, M., GÜLEZ, P., KAYSERİLİ, E., YENER, H., KORKMAZ, S. (2004). Crouzon Syndrome: Neonatal Case Report. Meandros Medical And Dental Journal, Cilt: 5 Sayı: 2, 27–29. https://ajindex.com/articles/1002893

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References (12)

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