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A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulated spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized.
No clinical trials have been registered for myelic limited dorsal malformation.
4 publications have been identified in PubMed for myelic limited dorsal malformation. Research spans Epidemiology / Natural History (50%), Other (25%), and Review / Meta-Analysis (25%).
Keil C (2026). [PMID: 41298113](https://pubmed.ncbi.nlm.nih.gov/41298113/). *Prenatal diagnosis*. [Other]
Kunpalin Y (2026). [PMID: 41419435](https://pubmed.ncbi.nlm.nih.gov/41419435/). *Prenatal diagnosis*. [Epidemiology / Natural History]
Dhombres F (2025). [PMID: 40629359](https://pubmed.ncbi.nlm.nih.gov/40629359/). *Orphanet journal of rare diseases*. [Review / Meta-Analysis]
Dugas A (2025). [PMID: 40237726](https://pubmed.ncbi.nlm.nih.gov/40237726/). *Prenatal diagnosis*. [Epidemiology / Natural History]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 10:22 PM UTC
European rare disease database