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Iniencephaly is a rare form of neural tube defect in which a malformation of the cervico-occipital junction is associated with a malformation of the central nervous system.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for iniencephaly.
4 publications have been identified in PubMed for iniencephaly. Research spans Case Report / Case Series (100%).
Gupta A (2025). [PMID: 39725026](https://pubmed.ncbi.nlm.nih.gov/39725026/). *Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC*. [Case Report / Case Series]
Minchola-Vega JL (2025). [PMID: 40740247](https://pubmed.ncbi.nlm.nih.gov/40740247/). *AJOG global reports*. [Case Report / Case Series]
Mendonça L (2024). [PMID: 39791056](https://pubmed.ncbi.nlm.nih.gov/39791056/). *Cureus*. [Case Report / Case Series]
Arega BN (2024). [PMID: 39726643](https://pubmed.ncbi.nlm.nih.gov/39726643/). *AJP reports*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:53 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center