Catalog

Familial scaphocephaly syndrome, McGillivray type

No MMS code

Link to WHO Definition

Familial scaphocephaly syndrome, McGillivray type – http://id.who.int/icd/entity/512057922

Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.