1.
Indian J Pathol Microbiol
; 47(2): 223-4, 2004 Apr.
Article
in English
| MEDLINE
| ID: mdl-16295475
ABSTRACT
Congenital factor X deficiency is a very rare inherited coagulation disorder. The clinical phenotype is of varying bleeding manifestations depending upon the level of factor activity. We describe a one and a half year old patient with severe deficiency (factor level less than 1%) who manifested with only easy bruisability and epistaxis that does not correlate with level of deficiency.