The appearance and gradual enlargement of fibrous cortical defects and multiple nonossifying fibromata are documented in
this report of a 2-year-old boy with a very rare skeletal dysplasia known as osteoglophonic dysplasia, characterized by multiple
and recurrent craniosynostoses, platyspondyly, short tubular bones, and epiphyseal dysplasia.
Received: 10 November 1995 Accepted: 13 March 1996