Please use this identifier to cite or link to this item:
https://ninho.inca.gov.br/jspui/handle/123456789/13921
Title: | Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome |
Authors: | Rodrigues, Eliane Ferreira Souza, Daiane Corrêa de Souza e Camargo, Adriana Tavares, Rita de Cássia Barbosa da Silva Bouzas, Luis Fernando da Silva Souza, Maria Helena Ornellas de Fernandez, Teresa de Souza |
Keywords: | Citogenética Cytogenetics Síndromes Mielodisplásicas Myelodysplastic Syndromes Transplante Transplantation child Criança Aberrações Cromossômicas Chromosome Aberrations |
Issue Date: | Oct-2007 |
Abstract: | A 13-year-old boy with hypocellular primary myelodysplastic syndrome, classified as refractory cytopenia, underwent umbilical cord blood transplantation. Cytogenetic analysis revealed two rare biclonal chromosomal aberrations, del(17)(p12) and del(11)(q23). Cytogenetic analysis was a valu able tool in diagnosis, in clinical decision-making, and in treatment and follow-up. To our knowl edge, this is the first reported case of cytogenetic biclonality involving chromosomes 17 and 11. |
URI: | https://ninho.inca.gov.br/jspui/handle/123456789/13921 |
ISSN: | 1873-4456 |
Appears in Collections: | Hospital do Câncer I (HCI) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome. 2007..pdf | 168.61 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.