Goldenhar Syndrome in a 9-year-old Patient - A Rare Case Report
The complex and rare condition known as Goldenhar syndrome (GHS) is characterized by mandibular hypoplasia, ear abnormalities, ocular dermoid and vertebral problems, and hemi facial macrosomia. The age of the patient and any systemic clinical manifestations will determine the treatment plan, which f...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Wolters Kluwer Medknow Publications,
2024-05-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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