The following Conditions are related to Webbed feet

Select a specific condition below to view its details.

  • Apert syndrome

    Apert syndrome, also known as acrocephalosyndactyly type I (ACS1), is a rare genetic disorder that is apparent at birth (congenital). The disorder is character-ized by distinctive malformations of the head that lead to distinctive facial features. In addition, the hands and/or feet may be webbed (syndactyly) and in some cases, mental retardation may also be present. Among babies born with Apert syndrome, the fibrous joints between  Read More

  • Syndactylic oxycephaly

    Apert syndrome, also known as acrocephalosyndactyly type I (ACS1), is a rare genetic disorder that is apparent at birth (congenital). The disorder is characterized by distinctive malformations of the head that lead to distinctive facial features. In addition, the hands and/or feet may be webbed (syndactyly) and in some cases, mental retardation may also be present. Among babies born with Apert syndrome, the fibrous joints between b  Read More