Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome

dc.Type	Article	pt_BR
dc.contributor.author	Rodrigues, Eliane Ferreira
dc.contributor.author	Souza, Daiane Corrêa de Souza e
dc.contributor.author	Camargo, Adriana
dc.contributor.author	Tavares, Rita de Cássia Barbosa da Silva
dc.contributor.author	Bouzas, Luis Fernando da Silva
dc.contributor.author	Souza, Maria Helena Ornellas de
dc.contributor.author	Fernandez, Teresa de Souza
dc.date.accessioned	2023-05-24T19:01:02Z
dc.date.available	2023-05-24T19:01:02Z
dc.date.issued	2007-10
dc.description.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.	pt_BR
dc.identifier.issn	1873-4456
dc.identifier.uri	https://ninho.inca.gov.br/jspui/handle/123456789/13921
dc.subject	Citogenética	pt_BR
dc.subject	Cytogenetics	pt_BR
dc.subject	Síndromes Mielodisplásicas	pt_BR
dc.subject	Myelodysplastic Syndromes	pt_BR
dc.subject	Transplante	pt_BR
dc.subject	Transplantation	pt_BR
dc.subject	child	pt_BR
dc.subject	Criança	pt_BR
dc.subject	Aberrações Cromossômicas	pt_BR
dc.subject	Chromosome Aberrations	pt_BR
dc.title	Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome	pt_BR

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