Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report

INTRODUCTION: Hereditary causes of visceral thrombosis or thrombosis should be sought among young patients. We present a case of a young man presenting with multiple hepatic infarctions resulting in portal hypertension due to homozygosity of the prothrombin gene mutation not previously described in...

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Detalles Bibliográficos
Autores principales: Emmanuelle, Theodore, Husein, Belkys, Iqbal, Javaid, Macheta, M, Isaacs, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2868876/
https://www.ncbi.nlm.nih.gov/pubmed/20429882
http://dx.doi.org/10.1186/1752-1947-4-122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2868876/
https://www.ncbi.nlm.nih.gov/pubmed/20429882
http://dx.doi.org/10.1186/1752-1947-4-122

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