Een familie met een autosomaal dominant overervende trombocytopenie

Tijdschrift voor Kindergeneeskunde

Volumn 65, Issue 1, 1997, Pages 35-38

  Ankum, M ^a   Van Kuppevelt, A J M ^b   Van Oostrom, C G ^c  

^a CANISIUS WILHELMINA HOSPITAL   (Netherlands)

^b Streekziekenhuis Koningin Beatrix ^*  (Netherlands)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0008239619     PISSN: 03767442     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

1. Najean Y, Lecompte T. Genetic trombocytopenia with autosomal dominant transmission: a review of 54 cases. Brit J Haematol 1990;74:203-8.
2. Nieuwenhuis HK. Chronische trombocytopenie. Ned Tijdschr Geneeskd 1988;132:1961-3.
3. Danielsson L, Jelf E, Lundkvist L. A new family with inherited thrombocytopenia. Scand J Haematol 1980;24:427-9.
4. Epstein CJ, Sahud MA, Piel CF, et al. Hereditary macrothrombocytopathia, nephritis and deafness. Am J Med 1972;52:299-310.
5. Kurstjens R, Bolt C, Vossen M, et al. Familial thrombopathic thrombocytopenia. Brit J Haematol 1968;15:305-17.
6. Carrington PA, Evans DIK, Cumming WJK, et al. Familial thrombocytopenia and myopathy Clin Lab Haematol 1989;11:323-9.
7. Bithell TC, Didisheim P, Cartwright GE, et al Thrombocytopenia inherited as an autosomal dominant trait. Blood 1965;25:231-40.
8. Cullum C, Cooney DP, Schrier SL. Familial thrombocytopenic thrombocytopathy. Brit J Haematol 1967;13:147-59.
9. Roberts MH, Smith MH. Thrombopenic purpura. Am J Dis Child 1950;79:820-5.
10. Myllylä G, Pelkonen R, Ikkala E, et al. Hereditary thrombocytopenia. Scand J Haematol 1967;4:441-52.
11. Greaves M, Pickering C, Martin J, et al. A new familial 'giant platelet syndrome' with structural, metabolic and functional abnormalities of platelets due to a primary megakaryocyte defect. Brit J Haematol 1987;65:429-35.
12. Murphy S, Oski FA, Gardner FH. Hereditary thrombocytopenia with an intrinsic platelet defect. N Engl J Med 1969;281:857-62.
13. Nathan DO, Oski FA. Haematology of infancy and childhood (4th edition), hoofdstuk 43. WB Saunders Company, 1993.
14. Dowton SB, Beardsley D, Jamison D, et al. Studies of a familial platelet disorder. Blood 1985;65:557-63.
15. Yufu Y, Ideguchi H, Narishige T, et al. Familial macrotrombocytopenia associated with decreased glycosylation of platelet membrane glycoprotein IV. Am J Hematol 1990;33:271-3.
16. Gardner FH, Bessman JD. Thrombocytopenia due to defective platelet production. Clin Haematol 1983;12:23-38.
17. Frojmovic MM, Milton JG. Human platelet size, shape, and related functions in health and disease. Physiol Rev 1982;62:185-261.
18. Murphy S. Hereditary thrombocytopenia. Clin Haematol 1972;1:359-68.
19. Godwin HA, Ginsburg AD. May-Hegglin anomaly: a defect in megakaryocyte fragmentation? Brit J Haematol 1974;26:117-28.
20. Behrens WE von. Mediterranean macro thrombocytopenia. Blood 1975;46:199-208.
21. Bain BJ, Seed M. Platelet count and platelet size in healthy Africans and West Indians. Clin Lab Haematol 1986;8:43-8.
22. Nieuwenhuis HK, Sixma JJ. Thrombocytopenia and the neglected megakaryocyte. N Eng J Med 1992;327:1812-3.
23. Gordon MS, Hoffman R. Growth factors affecting human thrombocytopoiesis: potential agents for the treatment of thrombocytopenia. Blood 1992;80:302-7.
24. Lee GR, et al Wintrobe's clinical hematology (9th edition), hoofdstuk 52,55,56. Lea & Febiger, 1993.