microcephaly, growth deficiency, seizures, and brain malformations (DOID:0081051)
Alliance: disease page
Alt IDs: OMIM:618346
Definition: A syndrome that is characterized by intrauterine growth retardation, postnatal growth deficiency with severe microcephaly, and poor or absent psychomotor development, and that has_material_basis_in homozygous mutation in the WDR4 gene on chromosome 21q22.