Add to ORKGCrouzon Syndrome is a rare genetic disorder resulting from a mutation of the Fibroblast Growth Factor Recep- tor 2 Gene. The main presenting feature of this syndrome is craniofacial synostosis but multiple physical dysmorphic features have been reported. There is a dearth of literature detailing the presentation of this syndrome in the foot and lower limb. Therefore, this case report will describe the clinical characteristics of a 22 year old female referred for podiatric assessment. It will also explore the possible treatment options considered for this case
Abstract Background FGFR2 encodes a fibroblast growth factor receptor whose mutations are responsibl...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
[[abstract]]Crouzon syndrome is an autosomal-dominant disorder that causes premature fusion of the c...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Crouzon syndrome is a genetic disorder, autosomal dominant, characterized by the premature fusion o...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
Introduction: The Crouzon syndrome or craniofacial dysostosis type I is a rare disease that affects ...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon syndrome is a rare disease, first decribed by Crouzon in 1912. This syndrome is cuased by mu...
The purposes of this study were to find a novel mutation of FGFR2 in Korean Crouzon syndrome patient...
Crouzon’s syndrome (CS) is a rare autosomal dominant condition with multiple mutations of the fibrob...
Crouzon syndrome is a rare autosomal dominant premature cranyosynostosis, caused by fibroblast growt...
Purpose: The purpose of this study was to investigate the fibroblast growth factor receptor 2 (FGFR2...
A human tail complicated by Crouzon syndrome is extremely rare, with only eight reported cases of hu...
Abstract Background FGFR2 encodes a fibroblast growth factor receptor whose mutations are responsibl...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
[[abstract]]Crouzon syndrome is an autosomal-dominant disorder that causes premature fusion of the c...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Crouzon syndrome is a genetic disorder, autosomal dominant, characterized by the premature fusion o...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
Introduction: The Crouzon syndrome or craniofacial dysostosis type I is a rare disease that affects ...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon syndrome is a rare disease, first decribed by Crouzon in 1912. This syndrome is cuased by mu...
The purposes of this study were to find a novel mutation of FGFR2 in Korean Crouzon syndrome patient...
Crouzon’s syndrome (CS) is a rare autosomal dominant condition with multiple mutations of the fibrob...
Crouzon syndrome is a rare autosomal dominant premature cranyosynostosis, caused by fibroblast growt...
Purpose: The purpose of this study was to investigate the fibroblast growth factor receptor 2 (FGFR2...
A human tail complicated by Crouzon syndrome is extremely rare, with only eight reported cases of hu...
Abstract Background FGFR2 encodes a fibroblast growth factor receptor whose mutations are responsibl...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
[[abstract]]Crouzon syndrome is an autosomal-dominant disorder that causes premature fusion of the c...