Catalog

Microcephaly-microcornea syndrome, Seemanova type

No MMS code

Link to WHO Definition

Microcephaly-microcornea syndrome, Seemanova type – http://id.who.int/icd/entity/1197077842

Microcephaly-microcornea syndrome, Seemanova type is characterised by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity.

Parents

LD20.2 Syndromes with microcephaly as a major feature
Syndromic conditions with disorders of intellectual development as a relevant clinical feature