Add to ORKGTo 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 retimlham...
We report a case of craniosynostosis showing spontaneous improvement in presumed superior oblique pa...
Background: A 13 year old boy presented with gradual poor grade in his school performance. Parents o...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...
Crouzon syndrome, also called craniofacial dysostosis is a rare autosomal dominant disease. It has a...
Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with comple...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
Crouzon syndrome (CS) is an autosomal dominant disorder characterized by craniofacial deformities ca...
Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynost...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
PurposeTo document the frequency of ophthalmic sequelae in patients with Crouzon syndrome before the...
Crouzon syndrome is the most common type of craniofacial dysostosis anomaly which presents a great c...
We report a case of craniosynostosis showing spontaneous improvement in presumed superior oblique pa...
Background: A 13 year old boy presented with gradual poor grade in his school performance. Parents o...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...
Crouzon syndrome, also called craniofacial dysostosis is a rare autosomal dominant disease. It has a...
Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with comple...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
Crouzon syndrome (CS) is an autosomal dominant disorder characterized by craniofacial deformities ca...
Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynost...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
PurposeTo document the frequency of ophthalmic sequelae in patients with Crouzon syndrome before the...
Crouzon syndrome is the most common type of craniofacial dysostosis anomaly which presents a great c...
We report a case of craniosynostosis showing spontaneous improvement in presumed superior oblique pa...
Background: A 13 year old boy presented with gradual poor grade in his school performance. Parents o...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...