Tag Archives: syndrome

Genetics Home Reference: craniofrontonasal syndrome

Craniofrontonasal syndrome is a rare condition characterized by the premature closure of certain bones of the skull (craniosynostosis) during development, which affects the shape of the head and face. The condition is named for the areas of the body that are typically affected: the skull (cranio-), face (fronto-), and nose (nasal). In people with craniofrontonasal… Read More »