> Detailanzeige

Schneppenheim, Reinhard; Budde, Ulrich; Oyen, Florian; Angerhaus, Dorothea; Aumann, Volker; Drewke, Elke; Hassenpflug, Wolf; Häberle, Johannes; Kentouche, Karim; Kohne, Elisabeth; Kurnik, Karin; Mueller-Wiefel, Dirk; Obser, Tobias; Santer, René; Sykora, Karl-Walter

von Willebrand factor cleaving protease and ADAMTS13mutations in childhood TTP

Literatur-
verwaltung

Zur
Merkliste

Lösche von
Merkliste

Per Whatsapp teilen

Schließen

Merkliste



Sie können Bookmarks mittels Listen verwalten, loggen Sie sich dafür bitte in Ihr SLUB Benutzerkonto ein.
  • Medientyp: E-Artikel
  • Titel: von Willebrand factor cleaving protease and ADAMTS13mutations in childhood TTP
  • Beteiligte: Schneppenheim, Reinhard; Budde, Ulrich; Oyen, Florian; Angerhaus, Dorothea; Aumann, Volker; Drewke, Elke; Hassenpflug, Wolf; Häberle, Johannes; Kentouche, Karim; Kohne, Elisabeth; Kurnik, Karin; Mueller-Wiefel, Dirk; Obser, Tobias; Santer, René; Sykora, Karl-Walter
  • Erschienen: American Society of Hematology, 2003
  • Erschienen in: Blood
  • Sprache: Englisch
  • DOI: 10.1182/blood-2002-08-2399
  • ISSN: 1528-0020; 0006-4971
  • Schlagwörter: Cell Biology ; Hematology ; Immunology ; Biochemistry
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:p>Thrombotic thrombocytopenic purpura (TTP) is caused by the persistence of the highly reactive high-molecular-weight multimers of von Willebrand factor (VWF) due to deficiency of the specific VWF-cleaving protease (VWF-CP) ADAMTS13, resulting in microangiopathic disease. The acquired form is caused by autoantibodies against VWF-CP, whereas homozygous or compound heterozygous mutations of ADAMTS13 are responsible for recessively inherited TTP. We investigated 83 children with hemolytic or thrombocytopenic episodes with or without additional neurologic symptoms or renal failure. The presumed diagnosis was chronic idiopathic thrombocytopenic purpura (ITP; n = 50), TTP (n = 8), hemolytic uremic syndrome (HUS; n = 24), and Evans syndrome (n = 1). A severe deficiency of VWF-CP (≤ 5%) was found in all investigated patients with TTP and in none of those with HUS. Additionally, 2 of 50 patients with a prior diagnosis of ITP were deficient for VWF-CP. Antibodies against VWF-CP were found in 4 children. Mutation analysis of the ADAMTS13 gene in the patients deficient in VWF-CP by direct sequencing of all 29 exons identified 8 different mutations, suggesting the hereditary form of TTP in 1 patient with ITP, in the patient with Evans syndrome, and in 5 of the 8 patients with TTP. The phenotype of TTP in childhood can be rather variable. Besides the classical clinical picture, oligosymptomatic forms may occur that can delay the identification of patients at risk.</jats:p>
  • Zugangsstatus: Freier Zugang