Congenital factor XIII deficiency: two case reports.

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Date
1991-04-01
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Abstract
Two 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.
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Pati 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): 347-8
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https://imsear.searo.who.int/handle/123456789/86917
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Journal of the Association of Physicians of India