Tag: Craniosynostosis
Syndactylic Oxycephaly
Syndactylic Oxycephaly: Definition and Description of Syndactylic Oxycephaly: Syndactylic Oxycephaly is a rare congenital condition characterized by the fusion of the fingers and/or toes (syndactyly) alongside craniosynostosis, which is the premature fusion of skull bones. This condition can result in distinctive facial features and abnormalities in head shape due to altered cranial and facial growth.…
Pfeiffer Syndrome Type I
Pfeiffer Syndrome Type I: Definition and Description of Pfeiffer Syndrome Type I: Pfeiffer Syndrome Type I, also known as classic Pfeiffer syndrome, is a genetic disorder characterized by the early fusion of certain skull bones, which affects head shape and can result in a number of associated physical symptoms. This condition is classified as a…
Craniosynostosis
Craniosynostosis Definition and Description of Craniosynostosis Craniosynostosis is a congenital condition characterized by the premature fusion of one or more cranial sutures—the fibrous joints connecting the bones of a baby’s skull. When these sutures close too early, it can restrict skull growth and result in an abnormal head shape. As the brain continues to grow,…
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…