Abstract
The Sack–Barabas syndrome, the vascular type of Ehlers–Danlos syndrome type IV, is considered the most serious form of Ehlers–Danlos syndrome as the vascular system is prone to aneurysmatic degeneration and rupture without preference of anatomic regions. We report a patient with Sack–Barabas syndrome who was treated by one vascular surgeon for 16 years, from the first of many operations until death at the age of 27.
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