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Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma.

Authors :
Oğur, G
Sengun, Z
Arel-Kiliç, G
Debusscher, Claire
Başaran, S
Ozbek, U
Ayan, I
Sariban, Eric
Vamos, E
Oğur, G
Sengun, Z
Arel-Kiliç, G
Debusscher, Claire
Başaran, S
Ozbek, U
Ayan, I
Sariban, Eric
Vamos, E
Source :
Cancer genetics and cytogenetics, 89 (1
Publication Year :
1996

Abstract

Two children with Klinefelter syndrome (KS), one associated with bilateral hereditary retinoblastoma (RB) and the other with rhabdomyosarcoma (RMS) are reported. Both were boys and chromosomally mosaic for KS. The hereditary retinoblastoma case yielded 46,XY,del(13)(q12q14.2)/47, XXY(c),del(13)(q12q14.2) in PHA-stimulated lymphocytes. The rhabdomyosarcoma case yielded 46,XY/ 47,XXY(c) in peripheral blood cells whereas tumor revealed trisomy 8, trisomy 7, and t(7;13)(q33;q32) in addition to 46,XY/47,XXyc mosaicism.<br />Case Reports<br />Journal Article<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
Cancer genetics and cytogenetics, 89 (1
Notes :
No full-text files, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1363679338
Document Type :
Electronic Resource