Catalog

Greig cephalopolysyndactyly syndrome

No MMS code

Link to WHO Definition

Greig cephalopolysyndactyly syndrome – http://id.who.int/icd/entity/606500237

Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterised by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands.