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Vascular Ehlers-Danlos syndrome is a rare hereditary connective tissue disease, the cause of which is a mutation in the COL3A1 gene.
Blood vessel
Recently, a research article was published in Stroke, an authoritative journal in the field of medsci.
medsci.
The study is a retrospective study conducted in a single-center cohort of patients with vascular Ehlers-Danlos syndrome confirmed by molecular testing at tertiary referral centers from 2000 to 2017.
144 patients were included in the study for analysis, 56.
It can be seen that carotid artery disease is very common in patients with vascular Ehlers-Danlos syndrome, and most of them have no clinical symptoms.
Carotid artery disease is common in patients with vascular Ehlers-Danlos syndrome, and most of them are asymptomatic.
Original source:
Salma Adham.
