LD20.3
category
Syndromes with holoprosencephaly as a major feature
Definition
Any syndrome caused by failure of the prosencephalon to divide in two during the antenatal period. These syndromes may present with closely spaced eyes, cyclopia, flat nasal bridge, single maxillary central incisor, small head size, and clefts of the lip and palate.
Also indexed as
Holoprosencephaly - craniosynostosisSyndromes with holoprosencephaly as a major featureXK aprosencephaly
Nearby in Syndromes with central nervous system anomalies as a major feature
LD20.0Syndromes with cerebellar anomalies as a major featureLD20.1Syndromes with lissencephaly as a major featureLD20.2Syndromes with microcephaly as a major featureLD20.4Syndromes with brain calcifications as a major feature4B4YOther specified diseases of the immune system4B4ZDiseases of the immune system, unspecified