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References
Sameer AS, Nissar S, Fatima K . Mismatch repair pathway: molecules, functions, and role in colorectal carcinogenesis. Eur J Cancer Prev 2014; 23: 246–257.
Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K et al. Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 2006; 296: 1479–1487.
Sehgal R, Sheahan K, O’Connell PR, Hanley AM, Martin ST, Winter DC . Lynch syndrome: an updated review. Genes 2014; 5: 497–507.
Wimmer K, Etzler J . Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of the iceberg? Hum Genet 2008; 124: 105–122.
Vasen HFA, Ghorbanoghli Z, Bourdeaut F, Cabaret O, Caron O, Duval A et alEU-Consortium Care for CMMR-D (C4CMMR-D). Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D). J Med Genet 2014; 51: 283–293.
Wang Q, Lasset C, Dessigne F, Frappaz D, Bergeron C, Navarro C et al. Neurofibromatosis and early onset cancers in hMLH-1-deficient children. Cancer Res 1999; 59: 294–297.
Elhasid R, Dvir R, Rosenfeld Keidar HR, Ben Shachar S, Bitan M, Solar I et al. Management of acute myeloblastic leukemia in a child with biallelic mismatch repair deficiency. J Pediatr Hematol Oncol 2015; 37: e490–e493.
Lavoine N, Colas C, Muleris M, Bodo S, Duval A, Entz-Werle N et al. Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort. J Med Genet 2015; 52: 770–778.
Ripperger T, Beger C, Rahner N, Sykora KW, Bockmeyer CL, Lehmann U et al. Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation. Haematologica 2010; 95: 841–844.
Bakry D, Aronson M, Durno C, Rimawi H, Farah R, Alharbi QK et al. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome; report from the constitutional mismatch repair deficiency consortium. Eur J Cancer 2014; 50: 987–996.
Wimmer K, Kratz CP, Vasen HF, Caron O, Colas C, Entz-Werle N et al. Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD). J Med Genet 2014; 51: 355–365.
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Heath, J., Campbell, M., Tiedemann, K. et al. Successful matched sibling cord blood transplant for ALL in a child with constitutional mismatch repair deficiency syndrome. Bone Marrow Transplant 51, 848–849 (2016). https://doi.org/10.1038/bmt.2015.353
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DOI: https://doi.org/10.1038/bmt.2015.353