hemifacial microsomia

(mi?kro-so'me-a),

HFM

A rare congenital anomaly, usually inherited sporadically, in which one side of the body, usually the right, fails to develop equally with the left. The ear, nose, and maxilla on the affected side are hypoplastic. In addition the right lung and kidney may be smaller than normal, and affected children often have ventriculoseptal defects. Surgical treatment of facial defects associated with HFM is often undertaken by combined teams of oral and maxillofacial surgeons. Synonym: facio-auriculo vertebral syndrome; Goldenhar syndrome; oculoauricular vertebral dysplasia

单词	hemifacial microsomia
释义	hemifacial microsomia hemifacial microsomia (mi?kro-so'me-a), HFM A rare congenital anomaly, usually inherited sporadically, in which one side of the body, usually the right, fails to develop equally with the left. The ear, nose, and maxilla on the affected side are hypoplastic. In addition the right lung and kidney may be smaller than normal, and affected children often have ventriculoseptal defects. Surgical treatment of facial defects associated with HFM is often undertaken by combined teams of oral and maxillofacial surgeons. Synonym: facio-auriculo vertebral syndrome; Goldenhar syndrome; oculoauricular vertebral dysplasia See HFM See HFM
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