Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease budd-chiari syndrome
Phenotype C0027022|myeloproliferative disorders
Sentences 2
PubMedID- 25698270 Diagnostic value of the jak2 v617f mutation for latent chronic myeloproliferative disorders in patients with budd-chiari syndrome and/or portal vein thrombosis.
PubMedID- 23837133 A clinical picture similar to that seen in the development of cardiac ascites is the hepatic venous outflow obstruction known eponymously as budd-chiari syndrome (bcs).27 causes of bcs include myeloproliferative disorders such as polycythemia vera and hypercoagulable states that stem from diseases such as systemic lupus erythematosis (sle) and paroxysmal nocturnal hemoglobinuria.

Page: 1