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Hypoprothrombinemia

A symptom of most likely a genetic disease, a disease process, or an adverse effect of a medication.

A deficiency of clotting factor II that leads to an increased physiological risk for bleeding, especially in the gastrointestinal system, cranial vault, and superficial integumentary system.

Peter M. Degel, BS, BSN, RN

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Gale Encyclopedia of Medicine : Coagulation disorders $5.99 Morbus hemorrhagicus neonatorum (hypoprothrombinemia neonatorum) (Acta paediatrica, vol. XXVII, supplementum I [i.e. 41])

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