A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience.
Indian J Hum Genet
; 2009 Sept; 15(3): 137-139
Article
de En
| IMSEAR
| ID: sea-138886
We report here two cases of trisomy 13 in acute myeloid leukemia M1 subtype. short-term unstimulated bone marrow and peripheral blood lymphocyte culture showed 47, XY, +13 in all metaphase plates and trisomy 13 was confirmed with whole chromosome paint probes. Trisomy 13 in AML-M1 is a rare numerical abnormality. This is the first Indian report of sole trisomy 13 in AML-M1. Here, we present two cases of elder male patients, which may constitute a distinct subtype.
Mots clés
Texte intégral:
1
Indice:
IMSEAR
Sujet Principal:
Trisomie
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Chromosomes humains de la paire 13
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Sujet âgé
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Humains
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Mâle
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Cellules de la moelle osseuse
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Lymphocytes
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Leucémie aigüe myéloïde
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Aberrations des chromosomes
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Hybridation fluorescente in situ
Pays comme sujet:
Asia
langue:
En
Texte intégral:
Indian j. hum. genet
Année:
2009
Type:
Article