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Thromb Haemost 2012; 107(03): 590-591
DOI: 10.1160/TH11-07-0474
DOI: 10.1160/TH11-07-0474
Letters to the Editor
A patient with Fechtner syndrome successfully treated with romiplostim
Weitere Informationen
Publikationsverlauf
Received:
13. Juli 2011
Accepted after major revision:
01. Januar 2011
Publikationsdatum:
22. November 2017 (online)
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References
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- 2 Kunishima S, Matsushita T, Kojima T. et al. Identification of six novel myh9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions. J Hum Genet 2001; 46: 722-729.
- 3 Seri M, Cusano R, Gangarossa S. et al. Mutations in myh9 result in the may-hegglin anomaly, and fechtner and sebastian syndromes. The may-heggllin/ fechtner syndrome consortium. Nat Genet 2000; 26: 103-105.
- 4 Pecci A, Gresele P, Klersy C. et al. Eltrombopag for the treatment of the inherited thrombocytopenia deriving from myh9 mutations. Blood 2010; 116: 5832-5837.
- 5 Savoia A, De Rocco D, Panza E. et al. Heavy chain myosin 9-related disease (myh9 -rd): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thromb Haemost 2010; 103: 826-832.
- 6 Kuter DJ, Mufti GJ, Bain BJ. et al. Evaluation of bone marrow reticulin formation in chronic immune thrombocytopenia patients treated with romiplostim. Blood 2009; 114: 3748-3756.
- 7 Kantarjian H, Fenaux P, Sekeres MA. et al. Safety and efficacy of romiplostim in patients with lower-risk myelodysplastic syndrome and thrombocytopenia. J Clin Oncol 2010; 28: 437-444.