Crouzon Syndrome.

• Main Authors: Rosarina, Dewi, soebagjo, Hendrian Dwikoloso
• Format: Article PeerReviewed
• Language: English; Indonesian
• Published: Airlangga University Press 2011
• Subjects: RE Ophthalmology
• Online Access: http://repository.unair.ac.id/53000/2/Peereview%209%20crouzon%20syndrome.pdf; http://repository.unair.ac.id/53000/13/53000.pdf; http://repository.unair.ac.id/53000/
• Institution: Universitas Airlangga

To report a c6e of patient with Crouzon syndrome. A case report, a 5 years old boy came to outpatient clinic with proptosh on his both eyes since binh . His parents also said the palate w6 deep and narrower than nomal. Emirulion of the ight eye releaved: visual acuity was 6/12 , intraocular pressure was norul palpation anterior seSment was proptosis, the other was within nomwl tirnit. Examination of the left eye revealed: visual acuity was 6/6, intraocular pressure was nomal palpation, anterior se*runt was proptosis, the other wu within normal limit. Ocular motility showed mild restriclion on both eyes. There was no strabhmus. Emmimtion of thefundus revealed: Fundal Rellexwu posilive, sharp mrgin optic disc with norul colour, no retimlhamorrhage, no bxudate, mcular reflex was positive. CT-scan emmination reyealed intemum lrydrocephalus, and there was no retrobulber mss. MRI emmimtion reyealed bilaterally aophthalmos, relatively ventriculomegaly caused by skull anonuly (orycephaly). Ptoptosis in this patient was caused by shallow orbits in crouzon syndromes. Radiological examination results a features showed patients with Crouzon syndrome. Crouzon syndrome is an exwnple of such a syndrome that is associated with premoture synostosis of the sutures of the skull, exophthalmos, head, orbit and jaw deformities.