Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern Iran

Blood Coagulation and Fibrinolysis

Volumn 22, Issue 5, 2011, Pages 396-401

  Mahmoodi, Mojtaba ^a,b   Peyvandi, Flora ^c   Afrasiabi, Abdolreza ^a   Ghaffarpasand, Fariborz ^d   Karimi, Mehran ^a  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b FASA UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c UNIVERSITY OF MILAN   (Italy)

^d SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

bleeding symptoms; coagulation disorders; heterozygous; southern Iran

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BERNARD SOULIER DISEASE; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 12 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CONGENITAL BLOOD CLOTTING DISORDER; FEMALE; FIBRINOGEN DEFECT; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HEMATOMA; HEMOPHILIA A; HETEROZYGOTE; HUMAN; HYPERMENORRHEA; IRAN; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; RETROSPECTIVE STUDY; VAGINA BLEEDING; VON WILLEBRAND DISEASE;

BLOOD COAGULATION DISORDERS, INHERITED; BLOOD PLATELET DISORDERS; COAGULATION PROTEIN DISORDERS; CROSS-SECTIONAL STUDIES; FEMALE; GENES, RECESSIVE; HEMORRHAGE; HETEROZYGOTE; HUMANS; IRAN; MALE; PREOPERATIVE CARE; RETROSPECTIVE STUDIES; VON WILLEBRAND DISEASE, TYPE 3;

EID: 79960698672     PISSN: 09575235     EISSN: 14735733     Source Type: Journal    
DOI: 10.1097/MBC.0b013e328345f566     Document Type: Article

References (26)

1. Konkle AB. Disorders of platelets and vessel wall. In Fauci AS, Braunwald E, Kasper DL, Hauser SL, Longo DL, Jameson JL, editors. Harrison's principles of internal medicine, 17th ed. New York: McGraw Hill; 2008 pp. 718-725
2. Mannucci PM, Tuddenham EG. The hemophilias: from royal genes to gene therapy. N Engl J Med 2001; 344:1773-1779 (Pubitemid 32497033)
3. Mannucci PM. Hemophilia: treatment options in the twenty-first century. J Thromb Haemost 2003; 1:1349-1355
4. Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002; 8:308-321 (Pubitemid 35277152)
5. Tuddenham EGD, Cooper DN. The molecular genetics of haemostasis and its inherited disorders. Oxford, United Kingdom: Oxford Medical Publications; 1994; Oxford Monography on Medical Genetics No. 25
6. Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood 2004; 104:1243-1252 (Pubitemid 39166494)
7. Peyvandi F, Tagliabue L,Menegatti M, Karimi M, Komáromi I, Katona E, et al. Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency. Hum Mutat 2004; 23:98
8. Kumar A, Mishra KL, Kumar A, Mishra D. Hereditary coagulation factor X deficiency. Indian Pediatr 2005; 42:1240-1242 (Pubitemid 43243957)
9. Karimi M, Yarmohammadi H, Ardeshiri R, Yarmohammadi H. Inherited coagulation disorders in southern Iran. Haemophilia 2002; 8:740-744 (Pubitemid 35446625)
10. Gupta PK, Charan VD, Saxena R. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders. Ann Hematol 2007; 86:403-407 (Pubitemid 46630057)
11. Acharya SS, Coughlin A, Dimichele DM. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VI, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2:248-256 (Pubitemid 40186038)
12. Dragani A, Malizia R, Iuliani O, Di Marzio I, Davì G. Inherited bleeding disorders: results from the Italian Regional Haemophilia Centre of Pescara. Blood Transfus 2008; 6:136-142 (Pubitemid 352031646)
13. Soucie JM, McAlister S, McClellan A, Oakley M, Su Y. The universal data collection surveillance system for rare bleeding disorders. Am J Prev Med 2010; 38 (4 Suppl):S475-S481
14. Eid SS, Kamal NR, Shubeilat TS, Wael AG. Inherited bleeding disorders: a 14-year retrospective study. Clin Lab Sci 2008; 21:210-214
15. Schlegel N, Bardet V, Kenet G, Muntean W, Zieger B, Nowak-Göttl U. Diagnostic and therapeutic considerations on inherited platelet disorders in neonates and children. Klin Padiatr 2010; 222:209-214
16. Al-Fawaz IM, Gader AM, Bahakim HM, Al-Mohareb F, Al-Momen AK, Harakati MS. Hereditary bleeding disorders in Riyadh, Saudi Arabia. Ann Saudi Med 1996; 16:257-261
17. Rick ME, Walsh CE, Key NS. Congenital bleeding disorders. Hematology Am Soc Hematol Educ Program 2003; 559-574
18. Israels SJ, El-Ekiaby M, Quiroga T, Mezzano D. Inherited disorders of platelet function and challenges to diagnosis of mucocutaneous bleeding. Haemophilia 2010; 16 (Suppl 5):152-159
19. Sajid R, Khalid S, Mazari N, Azhar WB, Khurshid M. Clinical audit of inherited bleeding disorders in a developing country. Indian J Pathol Microbiol 2010; 53:50-53
20. Karimi M, Haghpanah S, Amirhakimi A, Afrasiabi A, Dehbozorgian J, Nasirabady S. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory. Blood Coagul Fibrinolysis 2009; 20:642-645
21. International Registry of Rare Bleeding Disorders (RBDs), Luigi Villa Foundation, IRCSS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, University of Milan, A. Bianchi Bonomi Hemophilia and Thrombosis Center. Available from: http://www.rbdd.org. Accessed Aug 20, 2010
22. Karimi M, Menegatti M, Afrasiabi A, Sarikhani S, Peyvandi F. Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency. Haematologica 2008; 93:934-938 (Pubitemid 351821734)
23. Kadir RA, Economides DL, Sabin CA, Owens D, Lee CA. Frequency of inherited bleeding disorders in women with menorrhagia. Lancet 1998; 351
24. Hutspardol S, Sirachainan N, Soisamrong A, Atchararit N, O-Prasertsawat P, Chuansumrit A. Hemostatic defects in Thai adolescents with menorrhagia. J Med Assoc Thai 2010; 93:436-442
25. Gupta PK, Charan VD, Saxena R. Spectrum of Von Willebrand disease an inherited platelet function disorders amongst Indian bleeders. Ann Hematol 2007; 86:403-407 (Pubitemid 46630057)
26. Jayasinghe Y, Moore P, Donath S, Campbell J, Monagle P, Grover S. Bleeding disorders in teenagers presenting with menorrhagia. Aust N Z J Obstet Gynaecol 2005; 45:439-443 (Pubitemid 41830370)