Resource data
Cytogenetic study of 50 Brazilian patients with primary myelodysplastic syndrome
Fernandez,Teresa de Souza Silva,Maria Luiza M. Souza,Jamison M. de Tabak,Daniel Abdelhay,Eliana
Location:
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000100016
In this work we analyzed cytogenetically 50 patients with primary myelodysplastic syndrome from several hospitals of Rio de Janeiro, Brazil. The frequency of cytogenetic abnormalities was 32%. Patients with refractory anemia, or refractory anemia with ringed sideroblasts, presented normal karyotypes or single abnormalities such as del(5q) or -Y, while patients with refractory anemia with an excess of blasts, refractory anemia with an excess of blasts in transformation or chronic myelomonocytic leukemia showed complex karyotypes and single abnormalities involving chromosomes 7 or 8, which are related to a bad prognosis and an elevated risk of evolution to acute myeloid leukemia.
Belongs to: SciELO - Scientific Electronic Library Online
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Detalles del recurso
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Cytogenetic study of 50 Brazilian patients with primary myelodysplastic syndrome
|
| Id. |
506619 |
| Idioma |
inglés
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| Titulo |
Cytogenetic study of 50 Brazilian patients with primary myelodysplastic syndrome |
| Autor(es) |
Fernandez,Teresa de Souza Silva,Maria Luiza M. Souza,Jamison M. de Tabak,Daniel Abdelhay,Eliana |
| Location |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000100016
|
| Versión |
1.0 |
| Estado |
Final
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| Descripción |
In this work we analyzed cytogenetically 50 patients with primary myelodysplastic syndrome from several hospitals of Rio de Janeiro, Brazil. The frequency of cytogenetic abnormalities was 32%. Patients with refractory anemia, or refractory anemia with ringed sideroblasts, presented normal karyotypes or single abnormalities such as del(5q) or -Y, while patients with refractory anemia with an excess of blasts, refractory anemia with an excess of blasts in transformation or chronic myelomonocytic leukemia showed complex karyotypes and single abnormalities involving chromosomes 7 or 8, which are related to a bad prognosis and an elevated risk of evolution to acute myeloid leukemia. |
| Tipo |
text/html |
| Tipo de recurso |
journal article
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| Tipo de Interactividad |
Expositivo
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| Nivel de Interactividad |
muy bajo
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| Audiencia |
Estudiante
Profesor
Autor
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| Estructura |
Atomic |
| Coste |
no
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| Copyright |
sí
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| Formatos |
text/html |
| Requerimientos técnicos |
Browser: Any |
| Fecha de contribución |
22-may-2005 |
| Contacto |
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