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
The rare autosomal recessive form of the vascular type of Ehlers-Danlos syndrome. vEDS is almost always inherited in an autosomal dominant manner but rare examples of biallelic inheritance have been reported.
No clinical trials have been registered for autosomal recessive Ehlers-Danlos syndrome, vascular type.
6 publications have been identified in PubMed for autosomal recessive Ehlers-Danlos syndrome, vascular type. Research spans Case Report / Case Series (40%), Basic Science / Preclinical (40%), and Review / Meta-Analysis (20%).
AlAbdi L (2026). [PMID: 41887223](https://pubmed.ncbi.nlm.nih.gov/41887223/). *Am J Hum Genet*. [Basic Science / Preclinical]
Nakahara H (2026). [PMID: 42191857](https://pubmed.ncbi.nlm.nih.gov/42191857/). *J Hum Genet*. [Case Report / Case Series]
Merlini L (2025). [PMID: 40508193](https://pubmed.ncbi.nlm.nih.gov/40508193/). *Int J Mol Sci*. [Review / Meta-Analysis]
Dubacher N (2025). [PMID: 38950604](https://pubmed.ncbi.nlm.nih.gov/38950604/). *Thromb Haemost*. [Basic Science / Preclinical]
Gohal G (2025). [PMID: 40981013](https://pubmed.ncbi.nlm.nih.gov/40981013/). *Pediatr Rep*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 5:35 PM UTC