References
Smith OP, Hann IM, Woodward CE, Brockington M . Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA. Br J Haematol 1995; 90: 469–472.
Quinn CT, Kamen B . Pearson Syndrome. http://www.emedicine.com/ped/topic1750.htm. Accessed September 7, 2006.
Simonsz HJ, Barlocher K, Rotig A . Kearns–Sayre's syndrome developing in a boy who survived Pearson's syndrome caused by mitochondrial deletion. Doc Ophthalmol 1992; 82: 73–79.
Nieaudet P, Heidet L, Munnich A, Schmitz J . Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson's syndrome. Pediatr Nephrol 1994; 8: 164–168.
Superti-Furga E, Schoenle P, Tuschschmid R, Caduff R . Pearson's bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA. Eur J Pediatr 1993; 152: 44–50.
McKee DH, Cooper PN, Denning DW . Invasive aspergillosis in a patient with MELAS syndrome. J Neurol Neurosurg Psychiatry 2000; 68: 765–767.
Chu BC, Terae S, Takahashi C, Miyasaka K, Abe S . MRI of the brain in the Kearns–Sayre syndrome: report of four cases and a review. Neuroradiology 1999; 41: 759–764.
Slayton WB, Shibler KR . Congenital bone marrow failure syndrome associated with protean development defects and leukemia. Clin Perinatol 2000; 27: 543–558.
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This work was supported by the ‘Ministero della Salute – Ricerca Finalizzata Ministeriale’, ‘Fondazione CARIGE’, and ‘Compagnia San Paolo’.
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Faraci, M., Cuzzubbo, D., Micalizzi, C. et al. Allogeneic bone marrow transplantation for Pearson's syndrome. Bone Marrow Transplant 39, 563–565 (2007). https://doi.org/10.1038/sj.bmt.1705638
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DOI: https://doi.org/10.1038/sj.bmt.1705638
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