Monarch Disease Ontology term MONDO_0014714 (progressive microcephaly-seizures-cortical blindness-developmental delay syndrome) is a rare, genetic, neuro-ophthalmological syndrome characterized by post-natal, progressive microcephaly and early-onset seizures, associated with delayed global development, bilateral cortical visual impairment and moderate to severe intellectual disability. Additional manifestations include short stature, generalized hypotonia and pulmonary complications, such as recurrent respiratory infections and bronchiectasis. Auditory and metabolic screenings are normal. Also known as: SCBMS, seizures, cortical blindness, microcephaly syndrome.