Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Vascular ; 21(1): 43-5, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22871544

ABSTRACT

Ehlers-Danlos syndrome type 4, the vascular type, is a rare, life-threatening inherited disorder of the connective tissue. Affected patients are at risk of arterial, bowel and uterine rupture during pregnancy. Generally, this syndrome remains undiagnosed until a sudden, acute presentation with organ rupture, and results in premature death, even if the patients survive the first and second major complications. An early diagnosis with genetic assays can help to plan the best treatment, which is often challenging due to the frailty of the arterial tissue. We report on a 28-year-old lady who presented with spontaneous rupture of a pseudoaneurysm of the posterior tibial artery.


Subject(s)
Aneurysm, False/etiology , Aneurysm, Ruptured/etiology , Ehlers-Danlos Syndrome/complications , Tibial Arteries , Adult , Aneurysm, False/diagnosis , Aneurysm, False/surgery , Aneurysm, Ruptured/diagnosis , Aneurysm, Ruptured/surgery , Compartment Syndromes/etiology , Ehlers-Danlos Syndrome/diagnosis , Female , Hematoma/etiology , Humans , Rupture, Spontaneous , Tibial Arteries/diagnostic imaging , Tibial Arteries/surgery , Tomography, X-Ray Computed , Treatment Outcome
SELECTION OF CITATIONS
SEARCH DETAIL
...