Journals / İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi / 2014 / Cilt: 4 - Sayı: 1

A rare cardiac anomaly in Goldenhar’s syndrome: Isolated partial anomalous pulmonary venous return

Goldenhar sendromunda ender bir kardiyak anomali: İzole parsiyel pulmoner venöz dönüş anomalisi

Pages
69–71
DOI
—
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AI Summary & Key Takeaways

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

Here we present a case of a four months old female with Goldenhar’s syndrome and partial anomalous pulmonary venous return.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Goldenhar syndrome is a rare congenital abnormality characterized by incomplete development of the ear, nose, soft palate, lip, and mandible.
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Key Findings & Data:It is associated with anomalous development of the first and second branchial arch.
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Conclusion & Impact:Here we present a case of a four months old female with Goldenhar’s syndrome and partial anomalous pulmonary venous return.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Goldenhar syndrome is a rare congenital abnormality characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first and second branchial arch. Common clinical manifestations include limbal dermoids, preauricular skin tags, and strabismus. Here we present a case of a four months old female with Goldenhar’s syndrome and partial anomalous pulmonary venous return.

Özet

Goldenhar sendromu kulak, burun, yumuşak damak, dudak ve mandibulanın yetersiz gelişimiyle karakterize ender konjenital anomalidir. Birinci ve ikinci branşiyal arkın gelişim anomalisidir. Sık görülen belirtieri limbal dermoid, kulak önünde skin tag’ler, şaşılıkla karekterizedir. Burada biz 4 aylık bir kız çocuğunda izole parsiyel pumoner venöz dönüş anomalisini sunduk.

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Cite This Article

BALLI, Ş., ECE, İ., KİBAR, A. E., OFLAZ, M. B., BULUT, G. (2014). A rare cardiac anomaly in Goldenhar’s syndrome: Isolated partial anomalous pulmonary venous return. İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, Cilt: 4 - Sayı: 1, 69–71. https://ajindex.com/articles/210951

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References (10)

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