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Fig. 1 | BMC Ophthalmology

Fig. 1

From: Inherited FGFR2 mutation in a Chinese patient with Crouzon syndrome and luxation of bulbus oculi provoked by trauma: a case report

Fig. 1

Patients with Crouzon syndrome and clinical examination of the proband. a Three-generational Crouzon syndrome pedigree. Affected individuals are indicated by filled symbols and the proband is marked with an arrow. b, c Computed tomography and magnetic resonance imaging did not reveal retrobulbar hematoma and revealed shallow orbits and obvious ocular proptosis in the proband. d Facial photographs of patients with Crouzon syndrome

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BMC Ophthalmology

ISSN: 1471-2415

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