| Literature DB >> 7947285 |
H van Kamp1, J W Smit, E van den Berg, M Ruud Halie, E Vellenga.
Abstract
A patient with paroxysmal nocturnal haemoglobinuria (PNH) who developed a myelodysplastic syndrome (MDS) is described. After the onset of myelodysplasia the neutrophils of the patient fully expressed GPI-linked proteins. It is concluded that the myelodysplasia does not originate from transformed PNH stem cells, but represents the emergence of a separate clone arising from an injured marrow.Entities:
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Year: 1994 PMID： 7947285 DOI： 10.1111/j.1365-2141.1994.tb04929.x
Source DB: PubMed Journal: Br J Haematol ISSN： 0007-1048 Impact factor: 6.998