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A rare case of inherited factor‐II deficiency causing life‐threatening menorrhagia

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dc.contributor.author Sunita, T. H.
dc.contributor.author Desai, Rathnamala M.
dc.contributor.author Premaleela, K. G. M.
dc.date.accessioned 2013-07-11T21:03:23Z
dc.date.available 2013-07-11T21:03:23Z
dc.date.issued 2012-07
dc.identifier.citation Annals of Medical and Health Sciences Research. 2012 Jul; 2(2): 202-203. en_US
dc.identifier.issn 2141-9248, 2277-9205
dc.identifier.uri http://hdl.handle.net/123456789/426
dc.description.abstract Menorrhagia is a common gynecological symptom. In adolescents, the cause is generally dysfunctional uterine bleeding. Menorrhagia may also be due to undiagnosed coagulation defects, endocrine disorders, gynecological abnormalities of the uterus, or other systemic disorders. Menorrhagia may be the only clinical manifestation of an inherited bleeding disorder. We report a case of inherited hypoprothrombinemia (factor II deficiency), a rare bleeding disorder as the cause of life‐threatening menorrhagia. In the absence of a readily identifiable cause, all adolescents with menorrhagia should be examined for bleeding disorders. en_US
dc.language.iso en en_US
dc.publisher Wolters Kluwer-Medknow en_US
dc.subject Deficiency of clotting factors en_US
dc.subject Factor II deficiency en_US
dc.subject Menorrhagia en_US
dc.title A rare case of inherited factor‐II deficiency causing life‐threatening menorrhagia en_US
dc.type Article en_US


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