Diagnostic imageology of goldenhar syndrome: Report of a rare case
Goldenhar syndrome is a rare disorder that normally affects just one side and is distinguished by a variety of anomalies in internal organs, vertebrae, and craniofacial tissues. Although this sickness varies genetically and has been linked to a variety of factors, its etiology is unknown. We describ...
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| Príomhchruthaitheoirí: | , , , |
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| Formáid: | LEABHAR |
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Wolters Kluwer Medknow Publications,
2023-01-01T00:00:00Z.
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| Achoimre: | Goldenhar syndrome is a rare disorder that normally affects just one side and is distinguished by a variety of anomalies in internal organs, vertebrae, and craniofacial tissues. Although this sickness varies genetically and has been linked to a variety of factors, its etiology is unknown. We describe a case of hemifacial microsomia linked with Goldenhar syndrome that was clinically and radiographically investigated using cone-beam computed tomography. Several classical indications of the condition were present in the patient along with few uncommon ones. The many facets of this uncommon disease have been covered, with a focus on early detection and a multidisciplinary approach to treatment. |
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| Cur síos ar an mír: | 0976-237X 0976-2361 10.4103/ccd.ccd_180_23 |