Combined occurrence of von Willebrand's disease and factor XIII deficiency: a case report.

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dc.contributor.authorBatra, Vineeta Vijayen_US
dc.contributor.authorSaxena, Renuen_US
dc.contributor.authorSharma, Lalit Mohanen_US
dc.contributor.authorKashyap, Rajeshen_US
dc.contributor.authorChaudhry, Ved Prakashen_US
dc.date.accessioned2003-04-17en_US
dc.date.accessioned2009-05-29T13:37:32Z
dc.date.available2003-04-17en_US
dc.date.available2009-05-29T13:37:32Z
dc.date.issued2003-04-17en_US
dc.description.abstractWe report the case of a three year old female child with combined occurrence of von Willebrand's disease and factor XIII deficiency, an extremely rare combination. The patient presented with prolonged bleeding following cuts and wounds. Clot solubility test using 5M urea was positive. Platelet aggregation using ristocetin was reduced, which corrected on adding normal plasma. Aggregation with other agonists was normal. We discuss the clinico- hematological profile of the case. Only one such case has been reported in literature in the past to the best of our knowledge.en_US
dc.description.affiliationDepartment of Hematology, All India Institute of Medical Sciences, New Delhi. vvbatraa@2rediffmail.comen_US
dc.identifier.citationBatra VV, Saxena R, Sharma LM, Kashyap R, Chaudhry VP. Combined occurrence of von Willebrand's disease and factor XIII deficiency: a case report. Indian Journal of Pathology & Microbiology. 2003 Apr; 46(2): 217-9en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/75848
dc.language.isoengen_US
dc.source.urihttps://www.ijpmonline.orgen_US
dc.subject.meshChild, Preschoolen_US
dc.subject.meshFactor XIII Deficiency --blooden_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshvon Willebrand Disease --blooden_US
dc.titleCombined occurrence of von Willebrand's disease and factor XIII deficiency: a case report.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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