Rare bleeding disorders

Haemophilia

Volumn 12, Issue SUPPL. 3, 2006, Pages 137-142

  Peyvandi, Flora ^a   Kaufman, R J ^b   Seligsohn, U ^c   Salomon, O ^c   Boltoon Maggs, P H B ^d   Spreafico, M ^a   Menegatti, M ^a   Palla, R ^a   Siboni, S ^a   Mannucci, P M ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^c TEL AVIV UNIVERSITY   (Israel)

^d MANCHESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

Genetics; Guidelines; International Registry of RBDs; Rare bleeding disorders; RBDD; RBDs; Treatment

Indexed keywords

ANTITHROMBOCYTIC AGENT; BLOOD CLOTTING FACTOR 10A; BLOOD CLOTTING FACTOR 11A; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 7A; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9A; BLOOD CLOTTING FACTOR CONCENTRATE; DESMOPRESSIN; FIBRIN GLUE; FRESH FROZEN PLASMA; GAMMA GLUTAMYL HYDROLASE; TRANEXAMIC ACID; VITAMIN K GROUP;

ACUTE LUNG INJURY; ALLERGY; ANAPHYLAXIS; ARTERY THROMBOSIS; AUTOSOMAL RECESSIVE INHERITANCE; BLEEDING DISORDER; BLOOD CLOTTING FACTOR 11 DEFICIENCY; CAUTERIZATION; DATA BASE; FAMILY HISTORY; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENOTYPE; HEALTH HAZARD; HEART VALVE REPLACEMENT; HEMOLYSIS; HEMOPHILIA A; HEMOPHILIA B; HEMOSTASIS; HUMAN; HYPERVOLEMIA; KIDNEY DYSFUNCTION; LIVER DYSFUNCTION; MEDICAL AUDIT; MEDICAL INFORMATION SYSTEM; PATIENT ASSESSMENT; PRACTICE GUIDELINE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REGISTER; REVIEW; RISK ASSESSMENT; RISK FACTOR; SURGICAL RISK; SURGICAL TECHNIQUE; TOTAL HIP PROSTHESIS; TOTAL KNEE REPLACEMENT; TREATMENT PLANNING; VEIN THROMBOSIS; VIRUS INFECTION; VIRUS TRANSMISSION; VITAMIN K DEFICIENCY;

BLOOD COAGULATION DISORDERS, INHERITED; HUMANS; PRACTICE GUIDELINES; PRACTICE GUIDELINES AS TOPIC; REGISTRIES;

EID: 33646150228     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2006.01271.x     Document Type: Review

References (13)

1. 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).
2. Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002; 8: 308-21.
3. Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood 2004; 104: 1243-52.
4. Zhang B, Kaufman RJ, Ginsburg D. LMAN1 and MCFD2 form a cargo receptor complex and interact with coagulation factor VIII in the early secretory pathway. J Biol Chem 2005; 280: 25881-6.
5. MacLennan S, Barbara JA. Risks and side effects of therapy with plasma and plasma fractions. Best Pract Res Clin Haematol 2006; 19: 169-89.
6. Chandy M. Management of hemophilia with minimal factor replacement in developing countries: Role of ancillary therapy. Semin Thromb Hemost 2005; 31: 501-6.
7. Salomon O, Steinberg DM, Tamarin I, Zivelin A, Seligsohn U. Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency. Blood Coagul Fibrinolysis 2005; 16: 37-41.
8. Salomon O, Steinberg DM, Seligsohn U. Variable bleeding manifestation during different types of surgery in patients with severe factor XI deficiency support tailored replacement therapy. Submitted for publication 2006.
9. Asakai R, Chung DW, Davie EW, Seligsohn U. Factor XI deficiency in Ashkenazi Jews in Israel. N Engl J Med 1991; 325: 153-8.
10. Berliner S, Horowitz I, Martinowitz U, Brenner B, Seligsohn U. Dental surgery in patients with severe factor XI deficiency without plasma replacement. Blood Coagul Fibrinolysis 1992; 3: 465 -8.
11. Clinical PracticeOGuideline No. 1: Acute pain management: operative or medical procedures and trauma. Rockville (MD): US Department of Health and Human Services. Agency for Health Care Policy and Research; 1993. AHCPR Publication No. 92-0023. [cited 1993]
12. Bolton-Maggs PH, Perry DJ, Chalmers EA et al. The rare coagulation disorders -review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004; 10: 593-628.
13. Acharya S et al. Rare bleeding disorder Registry: Deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2: 248-56.