Fig. 1
From: An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome
Crouzon syndrome patients and morphology measurement of orbit. a Five-generation Crouzon syndrome pedigree. Affected individuals are indicated by filled symbols, the proband is marked with an upward arrow. b Facial photographs of the Crouzon syndrome patients. c Morphology measurement of orbit. (Ca) Three-dimensional reconstruction of skull of the proband IV-2 (Cb) Morphology measurement of orbit(a. midinterorbital distance, b.lateral orbital wall angle) (Cc) Morphology measurement of orbit(a. roof length, b. medial wall length, c. floor length, d. lateral wall length, e. orbital width, f. orbital height)