Add to ORKGThe most important craniofacial dysostosis & syndromes are Crouzon, Apret, Pfeiffer."nCarpenter Saether- Chotzen. The common characteristic is premature closure of cranial sutures, which"nresult in Maxillofacial deformities. Perfect recognition and carefully evaluation are the most important"npoints in their reconstruction surgery."nBecause the prevalence & surgical treatment of Crouzon syndrome is low, I present a case report include"nsurgical treatment of a patient with crouzon which was a accomplished in Shariati Hospital
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Introduction: The Crouzon syndrome or craniofacial dysostosis type I is a rare disease that affects ...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...
Crouzon syndrome is the most common type of craniofacial dysostosis anomaly which presents a great c...
Crouzon syndrome, also called craniofacial dysostosis is a rare autosomal dominant disease. It has a...
Objectives: The term Craniofacial dysostosis (CFD) is used to describe familiar forms of synostosis ...
Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with comple...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon syndrome (CS) is an autosomal dominant disorder characterized by craniofacial deformities ca...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynost...
The therapy of patients with Crouzon syndrome involves a multidisciplinary team. In most cases, this...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Introduction: The Crouzon syndrome or craniofacial dysostosis type I is a rare disease that affects ...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...
Crouzon syndrome is the most common type of craniofacial dysostosis anomaly which presents a great c...
Crouzon syndrome, also called craniofacial dysostosis is a rare autosomal dominant disease. It has a...
Objectives: The term Craniofacial dysostosis (CFD) is used to describe familiar forms of synostosis ...
Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with comple...
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying path...
Crouzon syndrome (CS) is an autosomal dominant disorder characterized by craniofacial deformities ca...
Abstract Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable ex...
Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynost...
The therapy of patients with Crouzon syndrome involves a multidisciplinary team. In most cases, this...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
Crouzon syndrome, a hereditary syndrome of craniofacial dysostosis, is a triad of skull deformities,...
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformation...
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivit...
Introduction: The Crouzon syndrome or craniofacial dysostosis type I is a rare disease that affects ...
Craniofacial dysostosis (Crouzon syndrome) is a syndrome characterized by premature closing of calva...