Literature DB >> 19592142

Bleeding in the heritable connective tissue disorders: mechanisms, diagnosis and treatment.

Fransiska Malfait1, Anne De Paepe.   

Abstract

Easy bruising and bleeding are prominent features of some heritable disorders of connective tissue (HDCT), resulting from fragility of capillaries and the perivascular connective tissue rather than clotting or platelet dysfunction. The bleeding tendency is most prominent in the Ehlers-Danlos syndrome (EDS), a heterogeneous group of HDCT sharing clinical manifestations of fragility in skin, ligaments, blood vessels and internal organs. Most EDS-subtypes are caused by mutations in genes encoding fibrillar collagens type I, III or V, or genes encoding enzymes involved in the posttranslational modification of collagens. In the vascular subtype of EDS, caused by defects in type III collagen, fragility of vessel walls can lead to life-threatening bleeding and premature death. Bleeding tendency is also a common feature in other EDS-subtypes, leading to bruising either spontaneously or after minimal trauma. This paper reviews the clinical aspects of bleeding and bruising in different HDCT and covers diagnostic and therapeutic aspects relevant to bleeding in these disorders.

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Year:  2009        PMID: 19592142     DOI: 10.1016/j.blre.2009.06.001

Source DB:  PubMed          Journal:  Blood Rev        ISSN: 0268-960X            Impact factor:   8.250


  11 in total

1.  Testicular torsion in a patient with Ehlers-Danlos syndrome.

Authors:  Amy Lee Fowler; David Bouchier Hayes; Eszter Feher
Journal:  BMJ Case Rep       Date:  2018-03-22

Review 2.  The bleeding child. Part I: primary hemostatic disorders.

Authors:  C Heleen van Ommen; Marjolein Peters
Journal:  Eur J Pediatr       Date:  2011-07-29       Impact factor: 3.183

3.  Lumbar artificial disc replacement in Ehlers-Danlos syndrome: A case report and discussion of clinical management.

Authors:  Emily M Lindley; Brianna N Patti; Matthew Taylor; Evalina L Burger; Vikas V Patel
Journal:  Int J Spine Surg       Date:  2012-12-01

4.  Rumpel-Leede phenomenon in a hypertensive patient due to mechanical trauma: a case report.

Authors:  Adam Hartley; Phang B Lim; Sajad A Hayat
Journal:  J Med Case Rep       Date:  2016-06-05

5.  Vascular type Ehlers-Danlos syndrome is associated with platelet dysfunction and low vitamin D serum concentration.

Authors:  Albert Busch; Sabine Hoffjan; Frauke Bergmann; Birgit Hartung; Helena Jung; Daniela Hanel; Andeas Tzschach; Janos Kadar; Yskert von Kodolitsch; Christoph-Thomas Germer; Heiner Trobisch; Erwin Strasser; René Wildenauer
Journal:  Orphanet J Rare Dis       Date:  2016-08-03       Impact factor: 4.123

6.  Dentinogenesis imperfecta type II in Swedish children and adolescents.

Authors:  K Andersson; B Malmgren; E Åström; G Dahllöf
Journal:  Orphanet J Rare Dis       Date:  2018-08-22       Impact factor: 4.123

7.  Fibronectin binding to von Willebrand factor occurs via the A1 domain.

Authors:  Daniel A Keesler; Tricia L Slobodianuk; Caroline E Kochelek; Chad W Skaer; Sandra L Haberichter; Veronica H Flood
Journal:  Res Pract Thromb Haemost       Date:  2021-06-05

Review 8.  Recommendations for anesthesia and perioperative management in patients with Ehlers-Danlos syndrome(s).

Authors:  Thomas Wiesmann; Marco Castori; Fransiska Malfait; Hinnerk Wulf
Journal:  Orphanet J Rare Dis       Date:  2014-07-23       Impact factor: 4.123

9.  Gynecologic symptoms and the influence on reproductive life in 386 women with hypermobility type ehlers-danlos syndrome: a cohort study.

Authors:  Justine Hugon-Rodin; Géraldine Lebègue; Stéphanie Becourt; Claude Hamonet; Anne Gompel
Journal:  Orphanet J Rare Dis       Date:  2016-09-13       Impact factor: 4.123

Review 10.  Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review.

Authors:  Sanne D'hondt; Tim Van Damme; Fransiska Malfait
Journal:  Genet Med       Date:  2017-10-05       Impact factor: 8.822

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