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A rare closed lipomatous, dysraphic malformation of the lower spinal cord characterized by extramedullary lipomatous mass attached to the conus region. The conus is dysplastic and poorly delineated. Various morphological subtypes are recognized. Possible symptoms include bowel and bladder dysfunction and neuro-orthopedic deformity of the lower limbs.
No clinical trials have been registered for extramedullary conus spinal cord lipoma.
2 publications have been identified in PubMed for extramedullary conus spinal cord lipoma. Research spans Review / Meta-Analysis (50%) and Case Report / Case Series (50%).
Kunpalin Y (2026). [PMID: 41419435](https://pubmed.ncbi.nlm.nih.gov/41419435/). *Prenatal diagnosis*. [Case Report / Case Series]
Dhombres F (2025). [PMID: 40629359](https://pubmed.ncbi.nlm.nih.gov/40629359/). *Orphanet journal of rare diseases*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 6:24 PM UTC
European rare disease database