A case of congenital bone marrow failure with radio-ulnar synostosis

International Journal of Hematology

Volumn 91, Issue 2, 2010, Pages 331-332

  Yoshida, Hisao ^a   Hashii, Yoshiko ^a   Okuda, Tokuko ^a   Kusuki, Shigenori ^a   Sato, Emiko ^a   Inoue, Akiko ^b   Kawakami, Chihiro ^b   Yabe, Miharu ^c   Ohta, Hideaki ^a   Ozono, Keiichi ^a  

^a OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b OSAKA MEDICAL COLLEGE   (Japan)

^c TOKAI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHOSPHAMIDE; FLUDARABINE; METHOTREXATE; TACROLIMUS;

ANEMIA; BONE MARROW BIOPSY; BONE MARROW DEPRESSION; BONE MARROW TRANSPLANTATION; BONE RADIOGRAPHY; CASE REPORT; CESAREAN SECTION; CHILD; CHROMOSOME ANALYSIS; DISEASE COURSE; FETUS HYDROPS; GESTATIONAL AGE; GRAFT VERSUS HOST REACTION; HUMAN; HUMAN TISSUE; IMMUNOSUPPRESSIVE TREATMENT; LETTER; MALE; NEUTROPENIA; OUTCOME ASSESSMENT; PRESCHOOL CHILD; RADIUS; SYNOSTOSIS; THROMBOCYTOPENIA; ULNA;

BLOOD TRANSFUSION; BONE MARROW; BONE MARROW DISEASES; BONE MARROW TRANSPLANTATION; HUMANS; INFANT, NEWBORN; MALE; RADIUS; THROMBOCYTOPENIA; ULNA;

EID: 77950918382     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12185-010-0494-z     Document Type: Letter

References (10)

1. CA Sieff E Nisbet-Brown DG Nathan 2000 Congenital bone marrow failure syndromes Br J Haematol 111 30 42 10.1046/j.1365-2141.2000.02263.x 1:STN:280:DC%2BD3M%2FltFahtQ%3D%3D 11091180
2. LK Diamond WC Wang BP Alter 1976 Congenital hypoplastic anemia Adv Pediatr 22 349 78 1:STN:280:DyaE287otFGgtA%3D%3D 773132
3. KL Greenhalgh RT Howell A Bottani PJ Ancliff HG Brunner CC Verschuuren-Bemelmans, et al. 2002 Thrombocytopenia-absent radius syndrome: a clinical genetic study J Med Genet 39 876 81 10.1136/jmg.39.12.876 1:STN:280:DC%2BD38jgvF2msA%3D%3D 12471199 (Pubitemid 36009148)
4. AA Thompson LT Nguyen 2000 Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation Nat Genet 26 397 8 10.1038/82511 1:CAS:528:DC%2BD3cXptVWgsbo%3D 11101832
5. FR Goodman 2002 Limb malformations and the human HOX genes Am J Med Genet 112 256 65 10.1002/ajmg.10776 12357469
6. B Argiropoulos RK Humphries 2007 Hox genes in hematopoiesis and leukemogenesis Oncogene. 26 6766 76 10.1038/sj.onc.1210760 1:CAS:528: DC%2BD2sXhtFKhsLnK 17934484 (Pubitemid 47585101)
7. B Favier FM Rijli C Fromental-Ramain V Fraulob P Chambon P Dollé 1996 Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton Development. 122 449 60 1:CAS:528:DyaK28Xhtlemt7g%3D 8625796 (Pubitemid 26054134)
8. FM Rijli P Chambon 1997 Genetic interactions of Hox genes in limb development: learning from compound mutants Curr Opin Genet Dev 7 481 7 10.1016/S0959-437X(97)80074-3 1:CAS:528:DyaK2sXlvV2ksrk%3D 9309178 (Pubitemid 27404278)
9. AA Thompson K Woodruff SA Feig LT Nguyen NC Schanen 2001 Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome Br J Haematol 113 866 70 10.1046/j.1365-2141.2001.02834.x 1:STN:280: DC%2BD3MzovVOnsg%3D%3D 11442476 (Pubitemid 32634751)
10. I Dokal P Ganly I Riebero J Marsh A Steed J Kendra, et al. 1989 Late onset bone marrow failure associated with proximal fusion of radius and ulna: a new syndrome Br J Haematol 71 277 80 10.1111/j.1365-2141.1989.tb04267.x 1:STN:280:DyaL1M7ms1ektQ%3D%3D 2923811 (Pubitemid 19061680)