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Table 1 Quantitative morphometry of the orbit in Crouzon syndrome patient and normal population [12]

From: An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome

  orbital width orbital height roof length floor length medial wall length lateral wall length ocular protrusion BOV Angle Midwinter orbital distance
  OD/OS OD/OS OD/OS OD/OS OD/OS OD/OS OD/OS OD/OS OD/OS
  mm mm mm mm mm mm mm ml degrees mm
Patient 44.94/ 43.60 39.16/38.60 49.66/ 48.09 37.38/34.66 39.97/38.00 44.65/42.62 24.59/23.85 17.15/16.31 56.52°/55.94° 40.01
Normal 33.35 ± 1.44 40.02 ± 1.63 52.93 ± 2.89 47.93 ± 2.68 46.32 ± 2.67 48.38 ± 2.50 16.97 ± 2.87 26.04 ± 2.60 42° 30
  1. Normal: 64 subjects who diagnose conditions other than craniofacial or orbital deformation