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Ehlers-Danlos, vascular-like type is an adult-onset form of Ehlers-Danlos syndrome characterized by spontaneous dissection of medium-sized arteries during young adulthood, including mainly the iliac, femoral, and renal arteries.
No clinical trials have been registered for Ehlers-Danlos syndrome, vascular-like type.
2 publications have been identified in PubMed for Ehlers-Danlos syndrome, vascular-like type. Research spans Other (50%) and Case Report / Case Series (50%).
Tanaka M (2024). [PMID: 39211523](https://pubmed.ncbi.nlm.nih.gov/39211523/). *Acute Med Surg*. [Case Report / Case Series]
Palomo-Toucedo IC (2024). [PMID: 39685014](https://pubmed.ncbi.nlm.nih.gov/39685014/). *Healthcare (Basel)*. [Other]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:51 AM UTC
European rare disease database
Common questions about Ehlers-Danlos syndrome, vascular-like type