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
Hauptverfasser:	Harel, Ronen, Shani, Dana, Donohoe, Kelsey
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Female Hemorrhagic Disorders - complications Humans Hypoprothrombinemias - complications Pregnancy Purpura, Thrombocytopenic, Idiopathic - complications
Online-Zugang:	Volltext
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