Inherited platelet function disorders versus other inherited bleeding disorders: An Indian overview

Thrombosis Research

Volumn 121, Issue 6, 2008, Pages 835-841

  Ahmad, Firdos ^a   Kannan, Meganathan ^a   Ranjan, Ravi ^a   Bajaj, Jyoti ^a   Choudhary, Ved P ^a   Saxena, Renu ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Bleeding disorders; India; Inherited; Platelet function defects; Prevalence

Indexed keywords

ARTICLE; BLEEDING DISORDER; BLOOD CLOTTING DISORDER; CORRELATION ANALYSIS; DISEASE SEVERITY; FEMALE; HEMOPHILIA A; HEMOPHILIA B; HOSPITAL ADMISSION; HUMAN; INDIAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; THROMBOCYTE ANOMALY; THROMBOCYTE FUNCTION; VON WILLEBRAND DISEASE;

ADULT; BLOOD COAGULATION DISORDERS, INHERITED; BLOOD PLATELET DISORDERS; FEMALE; HEMOSTASIS; HUMANS; INDIA; MALE; PREVALENCE; SEVERITY OF ILLNESS INDEX;

EID: 41749104247     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.thromres.2007.07.015     Document Type: Article

References (40)

1. Handin R.I. Inherited platelet disorders. Haematology 1 (2005) 396-402
2. Rao A.K., Jalagadugula G., and Sun L. Inherited defects in platelet signaling mechanisms. Semin Thromb Hemost 30 (2004) 525-535
3. Rao A.K. Congenital disorders of platelet secretion and signal transduction. In: Colman R.W., Hirsch J., Marder V.J., Clowes A., and George J.N. (Eds). Haemostasis and Thrombosis: Basic Principles and Clinical Practice (2001), J.B. Lippincott, Philadelphia 890-904
4. Nurden A.T. Qualitative disorders of platelets and megakaryocytes. J Thromb Haemost 3 (2005) 1773-1782
5. Cattaneo M. Inherited platelet abnormalities. Thromb Res 115 (2005) 10-13
6. Drachman J.G. Inherited thrombocytopenia: when a low platelet count does not mean ITP. Blood 103 (2004) 390-398
7. Geddis A.E., and Kaushansky K. Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production. Curr Opin Pediatr 16 (2004) 15-22
8. Cattaneo M. Inherited platelet-based bleeding disorders. J Thromb Haemost 1 (2003) 1628-1636
9. Hayward C.P. Inherited platelet disorders. Curr Opin Hematol 10 (2003) 362-368
10. Nurden A.T., and Nurden P. Inherited defects of platelet function. Rev Clin Exp Hematol 5 (2001) 314-334
11. Girolami A., Brunetti A., and Fioretti D. Congenital thrombocytopenia (Platelet factor 3 defect) with prolonged bleeding but normal platelet adhesiveness and aggregation. Acta Haematol 50 (1973) 116
12. Weiss H.J., Vicic W.J., and Lages B.A. Isolated deficiency of platelet procoagulant activity. Am J Med 67 (1979) 206
13. Hardisty R.M., and Hutton R.A. Platelet aggregation and availability of platelet factor 3. Br J Haematol 12 (1966) 764-766
14. Hardisty R.M., and Hutton R.A. Bleeding tendency associated with new abnormality of platelet behaviour. Lancet 1 (1967) 983
15. Weiss H.J. Platelet aggregation adhesion and ADP release in thrombopathia (platelet factor 3 deficiency) a comparison with Glanzmann thrombasthenia and von Willebrand disease. Am J Med 43 (1967) 570
16. Saxena R., Choudhry V.P., Mishra D.K., Kashyap R., Mohanty S., Mahapatra M., et al. Clinico-haematological profile of isolated PF3 availability defect: therapeutic potential of soya bean-a pilot study. Eur J Haematol 62 5 (May 1999) 327-331
17. 3) is a second mutation in Iraqi Jews that stemmed from a distinct founder. Blood 89 10 (1997) 3654-3662
18. Gupta M., Bhattacharyya M., Choudhry V.P., and Saxena R. Spectrum of inherited bleeding disorders in Indians. Clin Appl Thrombosis/Hemostasis 11 3 (2005) 325-330
19. Awidi A.S. Increased incidence of Glanzmann's thrombasthenia in Jordan as compared with Scandinavia. Scand J Haematol 30 (1983) 218
20. Newman P.J., Seligsohn U., Lyman S., and Coller B.S. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel. Proc Natl Acad Sci U S A 88 (1991) 3160
21. Mirghani A.M., and Ahmed M.O. Al-Sohaibani: inherited bleeding disorders in the eastern province of Saudi Arabia. Acta Haematol 79 (1988) 202
22. Schlegel N., Gayet O., Morel-Kopp M.C., Wyler B., Hurtaud-Roux M.F., Kaplan C., et al. The molecular genetic basis of Glanzmann's thrombasthenia in a Gypsy population in France: identification of a new mutation on the αIIb gene. Blood 86 (1995) 977
23. Seligsohn U., and Rososhansky S. A Glanzmann's thrombasthenia cluster among Iraqi Jews in Israel. Thromb Haemost 52 (1984) 230
24. Afshar-Kharghan V., and Lopez J.A. Bernard-Soulier syndrome caused by a dinucleotide deletion and reading frameshift in the region encoding the glycoprotein Ibα transmembrane domain. Blood 90 7 (1997) 2634-2643
25. Hayward C.P.M., Rao A.K., and Cattaneo M. Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment. Haemophilia 12 3 (2006) 128-136
26. Khanduri U., Pulimood R., Sudarsanam A., Carman R.H., Jadhav M., Pereira S., et al. Essential athrombia. A report on 4 cases from South India. Thromb Haemost 46 4 (Dec 23 1981) 722-724
27. Mannucci P.M., and Tuddenham E.G. The hemophilias from royal genes to gene therapy. N Engl J Med 344 (2001) 1773-1779
28. Mannucci P.M. Hemophilia: treatment options in the twenty-first century. J Thromb Haemost 1 (2003) 1349-1355
29. Sadler J.E., Mannucci P.M., Berntorp E., Bochkov N., Boulyjenkov V., Ginsburg D., et al. Impact, diagnosis and treatment of von Willebrand disease. Thromb Haemost 84 2 (Aug 2000) 160-174
30. Montgomery R.R., and Kroner P.A. von Willebrand disease: a common pediatric disorder. Pediatr Ann 30 (2001) 534-540
31. Peyvandi F., Duga S., Akhavan S., and Mannucci P.M. Rare coagulation deficiencies. Haemophilia 8 (2002) 308-321
32. Hassan A.A., and Kroll M.H. Acquired disorders of platelet function. Hematology 1 (2005) 403-408
33. Wazny L.D., and Ariano R.E. Evaluation and management of drug-induced thrombocytopenia in the acutely ill patient. Pharmacotherapy 20 3 (Mar 2000) 292-307
34. Dacie J.V., and Lewis S.M. Practical haematology. 9th ed. (2001), Churchill Livingstone, Edinburgh
35. Hayward C.P.M. Inherited disorders of platelet alphagranules. Platelets 8 (1997) 197-199
36. Khanduri U., Pulimood R., Sudarsanam A., Carman R.H., Jadhav M., and Pereira S. Glanzmann's thrombasthenia. A review and report of 42 cases from South India. Thromb Haemost 46 4 (Dec 23 1981) 717-721
37. Gupta P.K., Ahmad R.P.H., Sazawal S., Choudhry V.P., and Saxena R. Relatively high frequency of VWD type 3 and 2 in cohort of Indian patient: the role of multimeric analysis. J. Thromb Haemost 3 (2005) 1321-1322
38. Ahmed R.P., Ivaskevicius V., Kannan M., Seifried E., Oldenburg J., and Saxena R. Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A. Haematologica 90 2 (2005) 283-284
39. Kannan M., Ahmed R.P., Jain P., Kumar R., Choudhary V.P., and Saxena R. Type I Glanzmann thrombasthenia: most common subtypes in North Indians. Am J Hematol 74 2 (2003) 139-141
40. Lopez J.A., Andrews R.K., Affshar-Kharghan V., and Barandt4 M.C. Bernard Soulier syndrome. Blood 91 (1998) 4397-4418