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Rev Esp Enferm Dig ; 88(1): 43-5, 1996 Jan.
Article in Spanish | MEDLINE | ID: mdl-8616001

ABSTRACT

Ehlers-Danlos syndrome type IV is a heritable disease of type III collagen metabolism. Most patients have a defect either in the synthesis or structure of type III procollagen, a finding consistent with the fact that these patients are prone to spontaneous rupture of the aorta and intestines, tissues rich in type III collagen. The diagnosis is suspected in a patient with a combination of clinical manifestations and family history, but it is confirmed only by culture of the patient's skin fibroblasts and the demonstration of a defect in type III collagen metabolism. We present a patient with Ehlers-Danlos type IV syndrome who developed a recurrent colon perforation, and discuss the surgical strategy to prevent recurrences.


Subject(s)
Ehlers-Danlos Syndrome/complications , Intestinal Perforation/etiology , Sigmoid Diseases/etiology , Adult , Colon, Sigmoid/pathology , Ehlers-Danlos Syndrome/pathology , Female , Humans , Intestinal Perforation/pathology , Intestinal Perforation/surgery , Recurrence , Sigmoid Diseases/pathology , Sigmoid Diseases/surgery
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