Congenital factor XIII deficiency associated with von Willebrand disease.
Am J Hematol
; 35(3): 208-9, 1990 Nov.
Article
en En
| MEDLINE
| ID: mdl-2220766
ABSTRACT
A boy with umbilical bleeding and severe hemorrhages after minor trauma, without family bleeding history, was studied. Coagulation tests showed abnormalities in FXIII subunits and FVIII/vWF complex. Both parents presented results compatible with a heterozygote state for FXIII deficiency and the father had abnormalities of FVIII/vWF. The propositus was diagnosed as congenital FXIII deficiency associated with vWD. No severe hemorrhagic complication was observed after a prophylactic regimen with cryoprecipitates.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Enfermedades de von Willebrand
/
Deficiencia del Factor XIII
Tipo de estudio:
Diagnostic_studies
/
Risk_factors_studies
Límite:
Female
/
Humans
/
Infant
/
Male
Idioma:
En
Revista:
Am J Hematol
Año:
1990
Tipo del documento:
Article
País de afiliación:
Argentina