A case of congenital prothrombin deficiency and idiopathic thrombocytopenic purpura in a pregnant female
Hereditary prothrombin deficiency is an autosomal recessive disorder with an estimated incidence of 1 in 2 million [1]. Presentation of the disease is variable; however, it is usually associated with moderate to severe bleeding tendencies including muscle hematomas, hemarthrosis, intracranial, mucos...
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Veröffentlicht in: | Blood coagulation & fibrinolysis 2017-01, Vol.28 (1), p.100-101 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Hereditary prothrombin deficiency is an autosomal recessive disorder with an estimated incidence of 1 in 2 million [1]. Presentation of the disease is variable; however, it is usually associated with moderate to severe bleeding tendencies including muscle hematomas, hemarthrosis, intracranial, mucosal, and postoperative bleeding. Here we report a case of a 35-year-old pregnant woman with congenital hypoprothrombinemia and idiopathic thrombocytopenic purpura, review the literature, and discuss its epidemiology, presentation, diagnosis, and treatment. |
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ISSN: | 0957-5235 1473-5733 |
DOI: | 10.1097/MBC.0000000000000534 |