2007, Number 36
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Med Univer 2007; 9 (36)
Factor XIII deficency. Report of one case
Gerez MBP, González LO, Rodríguez RLN, Sandoval GAC, Marfil RLJ
Language: Spanish
References: 7
Page: 144-145
PDF size: 95.10 Kb.
ABSTRACT
Congenital Factor XIII deficiency was first described in 1960 and about 200 cases have been published about it. It is characterized by the appearance of delayed bleeding after suffering a trauma. It is diagnosed by demonstrating an increase in the solubility of a clot in urea and is confirmed by quantification of factor XIII. We report a 2-year-old patient with factor XIII deficiency. This is the first case seen in our hospital.
REFERENCES
Francis J, Todd P. Congenital factor XIII deficiency in a neonate. Br Med J 1978;2:1532.
Aziz MA, Siddigui AR. Congenital deficiency of fibrin-stabilizing factor (factor XIII): a report of four cases (two families) and family members. Blood 1972; 40:11-5.
Anwar R, Minford A, Gallivan L, Trinh C, Markham AF. Delayed umbilical bleeding¾a presenting feature for factor XIII deficiency: clinical features, genetics, and management. Pediatrics 2002;109:E32.
Newman RS, Jalili M, Kolls BJ, Dietrich R. Factor XIII deficiency mistaken for battered child syndrome: case of “correct” test ordering negated by a commonly accepted qualitative test with limited negative predictive value. Am J Hematol 2002;71:328-30.
Anwar R, Miloszewski KJ. Factor XIII deficiency. Br J Haematol 1999;107:468-84.
Ibrahim A, Kadankandy A, Mona B. Factor XIII deficiency in a Kuwaiti child: typical presentation with delayed diagnosis. Kuwait Medical Journal 2006;38:147-8.
García Arqueza C, Gutiérrez Benjumea A, Aguayo Maldonado J, Almuedo Paz A. Cephalohemoatoma como primera manifestación de déficit congénito de factor XIII. An Esp Pediatr 2000;53:241-2.