Congenital factor XIII deficiency: two case reports.

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dc.contributor.authorPati, H Pen_US
dc.contributor.authorChoudhry, V Pen_US
dc.contributor.authorArya, L Sen_US
dc.contributor.authorSaraya, A Ken_US
dc.date.accessioned1991-04-01en_US
dc.date.accessioned2009-05-30T19:35:37Z
dc.date.available1991-04-01en_US
dc.date.available2009-05-30T19:35:37Z
dc.date.issued1991-04-01en_US
dc.description.abstractTwo patients with factor XIII deficiency, presenting with bleeding disorder since birth, are reported. The condition is rare and is likely to be missed unless clot solubility in 5 M urea is performed as a screening test in all patients with bleeding disorders. A correct diagnosis is essential as prophylactic management is practicable in this disorder.en_US
dc.description.affiliationDepartment of Haematology, All India Institute of Medical Sciences, New Delhi.en_US
dc.identifier.citationPati HP, Choudhry VP, Arya LS, Saraya AK. Congenital factor XIII deficiency: two case reports. Journal of the Association of Physicians of India. 1991 Apr; 39(4): 347-8en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/86917
dc.language.isoengen_US
dc.source.urihttps://www.japi.orgen_US
dc.subject.meshAdulten_US
dc.subject.meshBlood Coagulation Testsen_US
dc.subject.meshChilden_US
dc.subject.meshFactor XIII Deficiency --congenitalen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.titleCongenital factor XIII deficiency: two case reports.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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