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Vascular type Ehlers-Danlos syndrome is associated with platelet dysfunction and low vitamin D serum concentration.
Busch, Albert; Hoffjan, Sabine; Bergmann, Frauke; Hartung, Birgit; Jung, Helena; Hanel, Daniela; Tzschach, Andeas; Kadar, Janos; von Kodolitsch, Yskert; Germer, Christoph-Thomas; Trobisch, Heiner; Strasser, Erwin; Wildenauer, René.
Afiliação
  • Busch A; Department for General, Visceral, Vascular & Paediatric Surgery, University Hospital of Würzburg - ZOM, Oberduerrbacher str 6, 97080, Würzburg, Germany. busch_a2@ukw.de.
  • Hoffjan S; Department of Human Genetics, Ruhr-University, Bochum, Germany.
  • Bergmann F; MVZ wagnerstibbe, amedes Gruppe, Hannover, Germany.
  • Hartung B; Institute of Clinical Chemistry, University Hospital Würzburg, Würzburg, Germany.
  • Jung H; Institute for medical genetics and molecular medicine, Cologne, Germany.
  • Hanel D; synlab MVZ Stuttgart GmbH, Stuttgart, Germany.
  • Tzschach A; Institute of Clinical Genetics, Technische Universität Dresden, Dresden, Germany.
  • Kadar J; UniversitätsCentrum für Seltene Erkrankungen, University Hospital Carl Gustav Carus, Dresden, Germany.
  • von Kodolitsch Y; Laboratory for Transfusion Medicine, Cologne, Germany.
  • Germer CT; Department of Cardiology, University Heart Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
  • Trobisch H; Department for General, Visceral, Vascular & Paediatric Surgery, University Hospital of Würzburg - ZOM, Oberduerrbacher str 6, 97080, Würzburg, Germany.
  • Strasser E; Laboratory and Ambulance for Coagulation Disorders, Duisburg, Germany.
  • Wildenauer R; Transfusion Medicine and Haemostaseology Department, University Hospital Erlangen, Erlangen, Germany.
Orphanet J Rare Dis ; 11(1): 111, 2016 08 03.
Article em En | MEDLINE | ID: mdl-27488172
BACKGROUND: The vascular type represents a very rare, yet the clinically most fatal entity of Ehlers-Danlos syndrome (EDS). Patients are often admitted due to arterial bleedings and the friable tissue and the altered coagulation contribute to the challenge in treatment strategies. Until now there is little information about clotting characteristics that might influence hemostasis decisively and eventually worsen emergency situations. RESULTS: 22 vascular type EDS patients were studied for hemoglobin, platelet volume and count, Quick and activated partial thromboplastin time, fibrinogen, factor XIII, von Willebrand disease, vitamin D and platelet aggregation by modern standard laboratory methods. Results show a high prevalence of over 50 % for platelet aggregation disorders in vascular type EDS patients, especially for collagen and epinephrine induced tests, whereas the plasmatic cascade did not show any alterations. Additionally, more than half of the tested subjects showed low vitamin D serum levels, which might additionally affect vascular wall integrity. CONCLUSION: The presented data underline the importance of detailed laboratory screening methods in vascular type EDS patients in order to allow for targeted application of platelet-interacting substances that might be of decisive benefit in the emergency setting.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vitamina D / Plaquetas / Síndrome de Ehlers-Danlos Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vitamina D / Plaquetas / Síndrome de Ehlers-Danlos Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article