Goldenhar Syndrome in a 6-Year-Old Patient: a Case Report and Review of Literature

Journal of Dentistry

Fatemeh Jahanimoghadam¹  Maryam Sharifi² 

[1] Oral and Dental Diseases Research Center, Kerman Social Determinants on Oral Health Research Center, Dept. of Pediatric Dentistry, School of Dentistry, Kerman University of Medical Sciences, Kerman, Iran. ;Resident Dept. of Pediatric Dentistry, School of Dentistry, Kerman University of Medical Sciences, Kerman, Iran. ;

关键词: craniofacial abnormalities● ventricular septal defects● mandibular condyle● oral manifestations● goldenhar syndrome;   

DOI  :  

来源: DOAJ

【 摘 要 】

Goldenhar syndrome (GHS) is a complex syndrome characterized by relation of mandibular hypoplasia, abnormality of the ear, ocular dermoid and vertebral disorders and hemi facial macrosomia. Treatment protocol depends on the patient’s age and systemic clinical presentations, with a multidisciplinary method often being required. This case report describes a typical 6-year-old female patient who presented to the Department of Pediatric Dentistry, Faculty of Dentistry, University of Medical Sciences, Kerman, Iran with mandibular hypoplasia, facial asymmetry, ear tags and ocular dermoid after plastic surgery. Diagnosis was based on clinical aspects, radiology and laboratory findings. GHS is a developmental complaint that can disturb many aspects of the patient's life; therefore, immediate treatment from birth is necessary.

【 授权许可】

Unknown