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- W2060185550 abstract "Ehlers-Danlos syndromes (EDSs) are heritable disorders of connective tissues leading to joint hypermobility, skin laxity, and tissue fragility. Of particular interest to gastroenterologists is the vascular type (previously known as type IV), which is characterized by spontaneous rupture of arterial and intestinal structures and increases the risk of diagnostic and therapeutic endoscopy. Here, we present a patient with suspected vascular-type EDS who safely underwent ERCP and sphincterotomy." @default.
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- W2060185550 date "2008-04-01" @default.
- W2060185550 modified "2023-09-24" @default.
- W2060185550 title "Successful ERCP and sphincterotomy in a patient with Ehlers-Danlos syndrome and a history of spontaneous bowel perforation" @default.
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- W2060185550 doi "https://doi.org/10.1016/j.gie.2007.09.013" @default.
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