Premature Craniosynostosis in a Rare Genetic Disease- A Case Report

• Main Authors: Hasnain Abbas Dharamshi (Author), Tufail Raza (Author), Ali Abbas Mohsin Ali (Author), Zuhair Lilani (Author), Syed Zohaib Ahsan (Author), Ahmad Faraz (Author), Syeda Tahira Naqvi (Author)
• Format: Book
• Published: Tehran University of Medical Sciences, 2015-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity.Its most notable characteristic feature is premature synostosis of cranial sutures .The case presented is of a 4 yr old boy with box like head with micr...