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Case Report

Goldenhar Syndrome: A Case Report

Sushruta Kumar, Habibur Rehman, Sunil Natha Mhaske, Abhijeet Shinde

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Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

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Indian Journal of Maternal-Fetal & Neonatal Medicine 9(1):p 25-27, january-June 2022. | DOI: https://doi.org/10.21088/ijmfnm.2347.999X.9122.3

How Cite This Article:

Habibur Rehman, Sushruta Kumar, Sunil Natha Mhaske, Abhijeet shinde/Goldenhar Syndrome: A Case Report /Indian Journal of Maternal-Fetal & Neonatal Medicine; 9(1):25–27

Timeline

Received : September 15, 2021         Accepted : October 19, 2021          Published : June 30, 2022

Abstract

Goldenhar syndrome is an uncommon disorder characterized by a variety of defects including craniofacial tissues, vertebrae, and internal organs. It preferably affects one side of the body. The origin of this illness is unknown because it is genetically variable and can be caused by a variety of factors. We present a case with Goldenhar syndrome with microtia, as well as systemic involvement, that was evaluated clinically and radiographically. The patient had many common symptoms of the illness as well as a few unusual ones. The many elements of this rare disease have been examined, with a focus on early detection and a multidisciplinary management strategy.


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Data Sharing Statement

There are no additional data available. All raw data and code are available upon request.

Funding

This research received no funding.

Author Contributions

All authors contributed significantly to the work and approve its publication.

Ethics Declaration

This article does not involve any human or animal subjects, and therefore does not require ethics approval.

Acknowledgements

We would like to express our gratitude to the patients, their families, and all those who have contributed to this study.

Conflicts of Interest

No conflicts of interest in this work.


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Cite this article

Habibur Rehman, Sushruta Kumar, Sunil Natha Mhaske, Abhijeet shinde/Goldenhar Syndrome: A Case Report /Indian Journal of Maternal-Fetal & Neonatal Medicine; 9(1):25–27


Licence:

Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


Received Accepted Published
September 15, 2021 October 19, 2021 June 30, 2022

DOI: https://doi.org/10.21088/ijmfnm.2347.999X.9122.3

Keywords

Goldenhar SyndromeRadiographicallyChromosome abnormalitiesMicrocornea

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Timeline


Received September 15, 2021
Accepted October 19, 2021
Published June 30, 2022

licence


Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


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