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)



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