1.
Indian J Pathol Microbiol
;
2004 Apr; 47(2): 259-61
Article
in English
| IMSEAR
| ID: sea-73694
ABSTRACT
Hereditary factor X deficiency is one of the rarest inherited coagulation factor deficiency. We are presenting here clinico-haematological profile and diagnostic approach of five such cases seen by us over a period of eleven years (year 1991-2001).
Subject(s)
Adolescent , Adult , Blood Coagulation Tests , Child, Preschool , Factor X Deficiency/blood , Humans , Male
2.
Indian J Pathol Microbiol
;
2004 Apr; 47(2): 223-4
Article
in English
| IMSEAR
| ID: sea-74194
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.
Subject(s)
Blood Coagulation Tests , Factor X Deficiency/blood , Humans , Infant , Male , Phenotype
3.
Southeast Asian J Trop Med Public Health
;
1979 Jun; 10(2): 251-4
Article
in English
| IMSEAR
| ID: sea-33555