Factor X deficiency--a rare disorder.

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dc.contributor.authorTrivedi, Sangitaen_US
dc.contributor.authorBhatia, Jurishen_US
dc.contributor.authorJain, Sumiten_US
dc.contributor.authorToprani, Tushar Hen_US
dc.date.accessioned2004-04-22en_US
dc.date.accessioned2009-05-29T12:04:07Z
dc.date.available2004-04-22en_US
dc.date.available2009-05-29T12:04:07Z
dc.date.issued2004-04-22en_US
dc.description.abstractCongenital factor X deficiency is a very rare inherited coagulation disorder. The clinical phenotype is of varying bleeding manifestations depending upon the level of factor activity. We describe a one and a half year old patient with severe deficiency (factor level less than 1%) who manifested with only easy bruisability and epistaxis that does not correlate with level of deficiency.en_US
dc.description.affiliationDepartment of Pathology, KGP Children Hospital and Jajodia Research Institute, Karelibaug, Vadodara. sangita_trivedi@hotmail.comen_US
dc.identifier.citationTrivedi S, Bhatia J, Jain S, Toprani TH. Factor X deficiency--a rare disorder. Indian Journal of Pathology & Microbiology. 2004 Apr; 47(2): 223-4en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/74194
dc.language.isoengen_US
dc.source.urihttps://www.ijpmonline.orgen_US
dc.subject.meshBlood Coagulation Testsen_US
dc.subject.meshFactor X Deficiency --blooden_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshMaleen_US
dc.subject.meshPhenotypeen_US
dc.titleFactor X deficiency--a rare disorder.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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