Literature DB >> 6613464

Vascular complications in the Ehlers-Danlos syndrome.

M Krog, B Almgren, I Eriksson, S Nordström.   

Abstract

The Ehlers-Danlos syndrome is a rare condition, which usually is easily recognized. In one type of this disease, type IV, arterial fragility dominates, and the syndrome may remain undiscovered until the patient has a traumatic or spontaneous arterial rupture. Two cases with a fatal outcome are presented in order to emphasize some important aspects in the management of these patients.

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Year:  1983        PMID: 6613464

Source DB:  PubMed          Journal:  Acta Chir Scand        ISSN: 0001-5482


  4 in total

1.  Spontaneous aortic rupture in a 22-year-old.

Authors:  M A Memon; C M Nicholson; J Clayton-Smith
Journal:  Postgrad Med J       Date:  1996-05       Impact factor: 2.401

Review 2.  Ehlers-Danlos syndrome and neurological features: a review.

Authors:  Salvatore Savasta; Pietro Merli; Martino Ruggieri; Lucia Bianchi; Maria Valentina Spartà
Journal:  Childs Nerv Syst       Date:  2010-08-10       Impact factor: 1.475

3.  Myocardial infarction resulting from coronary artery dissection in an adolescent with Ehlers-Danlos syndrome type IV due to a type III collagen mutation.

Authors:  L C Adès; R D Waltham; A A Chiodo; J F Bateman
Journal:  Br Heart J       Date:  1995-08

Review 4.  Successful coronary artery bypass in Ehlers-Danlos type IV syndrome case report and review of the literature.

Authors:  Hisham M F Sherif; Ray A Blackwell
Journal:  Tex Heart Inst J       Date:  2012
  4 in total

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