Goldenhar Syndrome: A Rare Case Report

Authors

  • Naznin Akther Assistant Professor, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Kaniz Fatema Assistant Registrar, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Jannatul Ferdush Chowdhury Assistant Professor, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Tofayel Ahmed Assistant Professor, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Zainab Rahman Registrar, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Rabaka Sultana IMO, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet

DOI:

https://doi.org/10.3329/jmj.v22i1.86510

Keywords:

Goldenhar syndrome, Microtia, Hemifacial microsomia, Epibulbar dermoid

Abstract

Goldenhar syndrome is a rare congenital condition characterised by a range of anomalies, including ear malformations, hemifacial microsomia, epibulbardermoids, vertebral anomalies, and potential internal organ defects. This syndrome arises from maldevelopment of the first and second branchial arches during early embryonic stages. Here we report a case of Goldenhar syndrome with congenital heart disease, bilateral microtia, and hemifacial microsomia.

Jalalabad Med J 2025; 22 (1): 37-39.

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Published

2026-01-04

How to Cite

Akther, N., Fatema, K., Chowdhury, J. F., Ahmed, T., Rahman, Z., & Sultana, R. (2026). Goldenhar Syndrome: A Rare Case Report. Jalalabad Medical Journal, 22(1), 37–39. https://doi.org/10.3329/jmj.v22i1.86510

Issue

Vol. 22 No. 1 (2025)

Section

Case Report

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Copyright (c) 2025 Jalalabad Medical Journal

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