Who is mostly affected by Jackson weiss syndrome?

Jackson-Weiss syndrome primarily affects individuals with genetic mutations that impact the development of bones and tissues in the skull and face. It is characterized by craniOSynostosis, which is the premature fusion of skull bones, along with other physical abnormalities. The syndrome can lead to various complications, affecting not only the physical appearance but also the function of the skull and facial structures. It is typically inherited in an autosomal dominant manner, meaning it can affect both males and females equally.