Combined factor VIII and IX deficiency in a family

Clinical and Laboratory Haematology

Volumn 23, Issue 3, 2001, Pages 201-204

  Shetty, S ^a   Ghosh, K ^a   Parekh, S ^b   Mohanty, D ^a  

^a KEM HOSPITAL   (India)

^b Hematology Laboratory   (India)

Author keywords

Combined; Factor deficiency; Haemophilia

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; DNA; VON WILLEBRAND FACTOR;

ADULT; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; DISEASE CARRIER; DNA DETERMINATION; FAMILIAL DISEASE; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC MARKER; HEMOPHILIA A; HEMOPHILIA B; HETEROZYGOTE DETECTION; HUMAN; MALE; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL;

ADULT; BLOOD COAGULATION TESTS; FAMILY HEALTH; HEMOPHILIA A; HEMOPHILIA B; HUMANS; MALE; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0035725163     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2257.2001.00381.x     Document Type: Article

References (13)

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3. Observations in a case of multiple hemostatic defect
4. Characterization of a variant prothrombin in a patient congenitally deficient in factors II, VII, IX and X
5. A female hemophilia A combined with hereditary coagulation factor XII deficiency
6. Report of a joint WHO/WFH meeting on the control of haemophilia. Carrier detection and prenatal diagnosis
7. Combined factor V and factor VIII deficiency: Report of 4 cases
8. Combined factor V and factor VIII deficiency in non ashkenazi Jews
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10. Familial multiple coagulation factors deficiencies
11. Combined antihaemophiliac globulin and Christmas factor deficiency in a haemophilia