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Endovascular repair of direct carotid–cavernous fistula in Ehlers–Danlos type IV

Ehlers–Danlos syndrome (EDS) type IV is a collagen vascular disease with an autosomal dominant inheritance caused by COL3A1 mutation. Patients with EDS type IV can present with organ rupture, spontaneous arterial dissections and ruptured aneurysms. Because of their propensity to form arterial dissec...

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Hlavní autoři: Linfante, Italo, Lin, Eugene, Knott, Eric, Katzen, Barry, Dabus, Guilherme
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3903160/
https://ncbi.nlm.nih.gov/pubmed/24385391
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-010990
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