Description
The syndrome shows a characteristic symmetrical, predominantly fronto-parietal distribution of polymicrogyria and specific calcification patterns in deep gray matter and basal ganglia. The molecular basis for this regional vulnerability despite ubiquitous OCLN expression is unknown.
Gap type: unexplained_observation Source paper: Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria. (None, None, PMID:28386946)