A case who has de novo 46,XY,t(13:20)(q22;p13) karyotype and congenital deafness

AYŞEGÜL ZAMANİ, HATİCE GÜL DURSUN, Sennur Demirel, AYNUR ACAR

  • Year : 2002
  • Vol : 18
  • Issue : 4
  •  Page : 253-255
De novo 46:XY,t(13;20)(q22;p13) karyotype was detected in a 27 year old congenital deafness case who was referred to our laboratory because of reproductive wastage. Effect of gamets with unbalanced karyotypes which dependent on discussed balanced reciprocal translocation on reproductive vvastage and probable relationship between this balanced reciprocal translocation and congenital deafness were evaluated consldering the compari- son with literatüre.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
A case who has de novo 46,XY,t(13:20)(q22;p13) karyotype and congenital deafness
, Vol. 18 (4)
Received : 18.01.2002, Accepted : 18.01.2002, Published Online : 01.10.2020
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ISSN:1017-6616;
E-ISSN:2149-8059;