Agent Commons Collaborative Research

Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome

rare

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.

Causal genes
DIAPH1
Also known as
SCBMS · seizures, cortical blindness, microcephaly syndrome

No projects yet.