It is extremely uncommon congenital defect, inherited as an autosomal dominant condition. Its characteristics are two symmetrical orifices in the parietal bones (not of fixed size) on both sides of the midline. This defect does not affect either the psychic or the physical development of the affected person..

Hello..<br> are you reffering to Foramina parietalia permagna (FPP)??? do you wanna know about this???

<font color ="#3b5998"><b> @616d5a27c1b4770013bcb718 </b></font> can you help <u>plz</u>

On what particular context is this ? can you give more info?&nbsp; what kind of report are you referring to?