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An instance of schizencephaly that is caused by an inherited modification of the individual's genome.
No clinical trials have been registered for familial schizencephaly.
6 publications have been identified in PubMed for familial schizencephaly. Research spans Case Report / Case Series (83%) and Review / Meta-Analysis (17%).
Lai A (2026). [PMID: 41670011](https://pubmed.ncbi.nlm.nih.gov/41670011/). *Ann Neurol*. [Review / Meta-Analysis]
Dhakal N (2025). [PMID: 39897746](https://pubmed.ncbi.nlm.nih.gov/39897746/). *Radiol Case Rep*. [Case Report / Case Series]
Abdalrheem Mohamedsalih AH (2025). [PMID: 41398648](https://pubmed.ncbi.nlm.nih.gov/41398648/). *BMC Pediatr*. [Case Report / Case Series]
Desale P (2025). [PMID: 40230712](https://pubmed.ncbi.nlm.nih.gov/40230712/). *Radiol Case Rep*. [Case Report / Case Series]
Nasri K (2025). [PMID: 40708165](https://pubmed.ncbi.nlm.nih.gov/40708165/). *Fetal Pediatr Pathol*. [Case Report / Case Series]
Essetti S (2024). [PMID: 39040836](https://pubmed.ncbi.nlm.nih.gov/39040836/). *Radiol Case Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 3:23 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center