A syndrome extent to heart from the ear: Goldenhar’s Syndrome

Kulaktan kalbe uzanan bir sendrom: Goldenhar Sendromu


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Authors

  • Sedat Işıkay Gaziantep Çocuk Hastanesi, Çocuk Nöroloji Kliniği, Gaziantep
  • Sadettin Sezer Gaziantep Çocuk Hastanesi, Çocuk Kardiyoloji Kliniği, Gaziantep
  • Ayşe Demirçubuk Gaziantep Çocuk Hastanesi, Yenidoğan Kliniği, Gaziantep
  • Evrim Kıray Baş Gaziantep Çocuk Hastanesi, Yenidoğan Kliniği, Gaziantep
  • Ünal Sarıkabadayı Gaziantep Çocuk Hastanesi, Yenidoğan Kliniği, Gaziantep

DOI:

https://doi.org/10.5455/GMJ-30-2013-145

Keywords:

Goldenhar syndrome, craniofacial abnormalities, microtia, facial asymmetry

Abstract

Goldenhar's syndrome or oculoauriculovertebral spectrum is a very rare disease, with characteristic oculo-auriculo-vertebral triad of abnormalities. In addition to craniofacial anomalies, there may be cardiac, genitourinary, skeletal and central nervous system defects. We report here a newborn presented with hypoplasia of depressor anguli oris muscle, microtia, vertebral fusion abnormality, pes equinovarus deformity and ventricular septal defect and diagnosed oculoauriculovertebral spectrum. In conclusion, Goldenhar’s syndrome may be observed in patients with ear anomalies and facial anomalies. The cases should be evaluated in terms of anomalies that may accompany.

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References

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Published

2023-05-01

How to Cite

Işıkay, S., Sezer, S., Demirçubuk, A., Kıray Baş, E., & Sarıkabadayı, Ünal. (2023). A syndrome extent to heart from the ear: Goldenhar’s Syndrome: Kulaktan kalbe uzanan bir sendrom: Goldenhar Sendromu. European Journal of Therapeutics, 19(3), 196–198. https://doi.org/10.5455/GMJ-30-2013-145

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Section

Case Reports