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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
Full text How to cite this article

Language: Spanish
References: 7
Page: 144-145
PDF size: 95.10 Kb.


Key words:

Factor XIII deficiency, bleeding disorder, unexplained hemorrhage.

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

  1. Francis J, Todd P. Congenital factor XIII deficiency in a neonate. Br Med J 1978;2:1532.

  2. 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.

  3. 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.

  4. 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.

  5. Anwar R, Miloszewski KJ. Factor XIII deficiency. Br J Haematol 1999;107:468-84.

  6. 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.

  7. 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.




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Med Univer. 2007;9