Catalog

XK aprosencephaly

No MMS code

Link to WHO Definition

XK aprosencephaly – http://id.who.int/icd/entity/1805259428

XK aprosencephaly represents the syndromic form of aprosencephaly and is characterised by near total absence of the prosencephalon with a midline oculofacial defect similar to that observed in the most severe forms of holoprosencephaly.