The O.M.E.N.S. classification of hemifacial microsomia

Cleft Palate Craniofac J. 1991 Jan;28(1):68-76; discussion 77. doi: 10.1597/1545-1569_1991_028_0068_tomens_2.3.co_2.

Abstract

The wide spectrum of anomalies associated with hemifacial microsomia (HFM) has made systematic and inclusive classification difficult. We propose a nosologic system in which each letter of the acronym O.M.E.N.S. indicates one of the five major manifestations of HFM. O for orbital distortion; M for mandibular hypoplasia; E for ear anomaly; N for nerve involvement; and S for soft tissue deficiency. The O.M.E.N.S. system is easily adapted for data storage, retrieval, and statistical analysis. A retrospective study of 154 patients with HFM classified according to the O.M.E.N.S. system confirmed the concept that the mandibular deformity is the cornerstone of the anomaly. Statistical analysis demonstrated a positive association between mandibular hypoplasia and the severity of orbital, auricular, neural, and soft tissue involvement. This study did not confirm a previously reported predominance of gender or sidedness. Analysis of statistical correlations failed to substantiate a Goldenhar variant as a syndromic entity. Our analysis showed that palatal deviation is probably caused by muscular hypoplasia and not by weakness of a particular cranial nerve.

MeSH terms

  • Adult
  • Child
  • Child, Preschool
  • Ear, External / abnormalities
  • Ear, External / pathology
  • Facial Asymmetry / classification*
  • Facial Asymmetry / pathology
  • Facial Muscles / abnormalities
  • Facial Muscles / pathology
  • Facial Nerve / physiopathology
  • Female
  • Humans
  • Male
  • Mandible / abnormalities
  • Mandible / pathology
  • Orbital Diseases / pathology
  • Peripheral Nervous System Diseases / physiopathology
  • Retrospective Studies