1.
Indian J Pathol Microbiol
;
2004 Apr; 47(2): 223-4
Article
Dans Anglais
| IMSEAR
| ID: sea-74194
Résumé
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.
Sujets)
Tests de coagulation sanguine , Déficit en facteur X/sang , Humains , Nourrisson , Mâle , Phénotype
2.
Indian J Pathol Microbiol
;
2004 Apr; 47(2): 259-61
Article
Dans Anglais
| IMSEAR
| ID: sea-73694
Résumé
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).
Sujets)
Adolescent , Adulte , Tests de coagulation sanguine , Enfant d'âge préscolaire , Déficit en facteur X/sang , Humains , Mâle
3.
Southeast Asian J Trop Med Public Health
;
1979 Jun; 10(2): 251-4
Article
Dans Anglais
| IMSEAR
| ID: sea-33555