Muenke Syndrome (genetic association)

Muenke Syndrome is a genetic condition caused by mutations in the FGFR3 gene. This disorder primarily affects the development of the skull and face, leading to features like a wide forehead and closely spaced eyes. It often results in early closure of the cranial sutures, known as craniosynostosis, which can affect head shape and brain growth. Other symptoms may include hearing problems and developmental delays. It is often inherited in an autosomal dominant pattern, meaning only one copy of the mutated gene from a parent is needed for a child to have the syndrome.