"absent/delayed ossification of the pubic bone creating the appearance of a pseudo-widening of the symphysis pubis"
"It is a rare polyostotic skeletal dysplasia caused by a mutation in the CBFA1 (also known as RUNX2) gene in AD inherited or sporadic mutation pattern (in approximately 40%) which is characterised by incomplete intramembranous ossification of midline skeletal structures inclusive of the clavicle as well as a defective development of the pubic bones, vertebral column, and long bones 5,6."
Expected headings
"Skull"
"Chest"
"Pelvis"
"Limbs"