X;6 translocation in a child with congenital acute lymphocytic leukemia.

Abstract:

:A case of congenital acute lymphoblastic leukemia (ALL) displayed an X;6 translocation. This is the third reported case of ALL with an X;6 translocation. In addition, two of the three ALL cases occurred during infancy, at ages 2 months and newborn, and both translocations involved the band q15-16 region of chromosome 6. Anomalies of the long arm of chromosome 6, mainly interstitial and terminal deletions, have been reported as a recurrent karyotypic event in a significant number of ALL cases. The molecular basis and propensity of an X;6 rearrangement in this case of congenital ALL is unclear and merits further investigation. The similarities in this case and the other infant ALL case cited suggest that an X;6 rearrangement with a breakpoint in bands q15-16 of chromosome 6 is characteristic of a form of congenital ALL.

journal_name

Cancer

journal_title

Cancer

authors

Carney LA,Kinney JS,Higgins RR,Freeman AI,Hecht BK,Woods GM

doi

10.1002/1097-0142(19920201)69:3<799::aid-cncr28206

subject

Has Abstract

pub_date

1992-02-01 00:00:00

pages

799-803

issue

3

eissn

0008-543X

issn

1097-0142

journal_volume

69

pub_type

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