Your browser doesn't support javascript.
loading
[Thrombotic microangiopathies]. / De trombotiske mikroangiopatier.
Nielsen, Ove Juul; Friis-Hansen, Lennart.
Affiliation
  • Nielsen OJ; Klinisk Biokemisk Afdeling KB3011, Rigshospitalet, DK-2100 København Ø, Denmark.
Ugeskr Laeger ; 171(49): 3614-20, 2009 Nov 30.
Article in Da | MEDLINE | ID: mdl-19954703
ABSTRACT
The thrombotic microangiopathic diseases, which include acquired and congenital TTP and HUS, are most frequently acute disease entities. Untreated, these diseases are associated with a lethal course in many cases. Deficiency of the von Willebrand cleaving enzyme, ADAMTS13, is a decisive pathophysiological defect in most cases of thrombotic microangiopathic diseases. Early recognition and a secure distinction from other conditions that resemble TMA diseases is essential in order to institute adequate treatment and to obtain a favourable outcome in terms of both survival and development of serious sequelae.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Thrombotic Microangiopathies Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Limits: Humans Language: Da Journal: Ugeskr Laeger Year: 2009 Document type: Article Affiliation country: Denmark
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Thrombotic Microangiopathies Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Limits: Humans Language: Da Journal: Ugeskr Laeger Year: 2009 Document type: Article Affiliation country: Denmark