Tag: FGFR1

  • Classic Type Pfeiffer Syndrome

    Classic Type Pfeiffer Syndrome Definition and Description of Classic Type Pfeiffer Syndrome Classic Type Pfeiffer Syndrome is a congenital disorder characterized by the premature fusion of certain cranial sutures, leading to an abnormal head shape and facial features. This condition falls under the category of syndromic craniosynostosis and primarily affects the skull, resulting in a…

  • Apert Syndrome

    Apert Syndrome Definition and Description of Apert Syndrome Apert Syndrome is a congenital disorder characterized by the premature fusion of certain skull bones, known as craniosynostosis. This condition affects the development of the skull, which can lead to an abnormal head shape and facial features. Individuals with Apert Syndrome may also experience fusion of fingers…