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

BMC Medical Genetics

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

	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	Midwinter orbital distance
	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

Normal: 64 subjects who diagnose conditions other than craniofacial or orbital deformation

ISSN: 1471-2350