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PedAM

Pediatric Disease Annotations & Medicines




Disease budd-chiari syndrome
Phenotype C0027022|myeloproliferative disorder
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.

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