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Journals / Bakırköy Tıp Dergisi / 2013 / Cilt: 9 - Sayı: 3

Goldenhar’ s syndrome: case report

Goldenhar Sendromu: Olgu Sunumu

Ali KARAMAN
Fuat LALOĞLU
Hasan KAHVECİ
Pages
131–133
DOI
—
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AI Summary & Key Takeaways

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

In this paper we report the clinical and laboratory findings of a patient with Goldenhar’s syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Goldenhar’s syndrome is a rare congenital syndrome characterized with ear, cardiac, and vertebral anomalies, facial asymmetria, epibulbar and dermoid cysts.
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Key Findings & Data:The incidence is around 1/5600 a live birth.
💡
Conclusion & Impact:In this paper we report the clinical and laboratory findings of a patient with Goldenhar’s syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Goldenhar’s syndrome is a rare congenital syndrome characterized with ear, cardiac, and vertebral anomalies, facial asymmetria, epibulbar and dermoid cysts. The incidence is around 1/5600 a live birth. The patients with Goldenhar’s syndrome may refer with minor or major abnormalities. In this paper we report the clinical and laboratory findings of a patient with Goldenhar’s syndrome.

Özet

Goldenhar sendromu kulak, kalp ve vertebra anomalileri, fasiyal asimetri, dermal ve epibulbar kistler ile karakterize, nadir görülen konjenital bir sendromdur. İnsidansı canlı doğumlarda yaklaşık olarak 1/5600’dir. Goldenhar sendromlu hastalar ağır anomaliler ya da daha hafif anomaliler ile başvurabilir. Bu yazıda Goldenhar sendromlu bir hastanın klinik ve laboratuvar bulgularını sunduk.

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Cite This Article

KARAMAN, A., LALOĞLU, F., KAHVECİ, H. (2013). Goldenhar’ s syndrome: case report. Bakırköy Tıp Dergisi, Cilt: 9 - Sayı: 3, 131–133. https://ajindex.com/articles/136673

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