Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Leptomyelolipoma is a rare neural tube closure defect characterized by an abnormally low lying conus which is tethered by a lumbosacral lipomatous mass (containing fatty tissue, nerve fibers, meningeal strands and fibrous bands) which engulfs the filum terminale and varying numbers of dorsal and ventral nerve root components, typically producing sensory, motor, bowel and/or bladder dysfunction. Cutaneous stigmata, absent or reduced reflexes and foot defomities (e.g. talipes cavovalgus) are frequently present.
No clinical trials have been registered for leptomyelolipoma.
1 publication has been identified in PubMed for leptomyelolipoma. Research spans Other (100%).
Dhombres F (2025). [PMID: 40629359](https://pubmed.ncbi.nlm.nih.gov/40629359/). *Orphanet J Rare Dis*. [Other]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 12:38 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center