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

  • AYŞEGÜL ZAMANİ: NECMETTİN ERBAKAN ÜNİVERSİTESİ
  • HATİCE GÜL DURSUN: SELÇUK ÜNİVERSİTESİ
  • Sennur Demirel: Selçuk Üniversitesi Meram Tıp Fakültesi
  • AYNUR ACAR: SELÇUK ÜNİVERSİTESİ
  • 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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Conflict of interest : Yok
This article is published under the CC BY-NC 4.0 license.
Selcuk Medical Journal
2002, Vol. 18 (4)
ISSN: 1017-6616
E-ISSN: 2149-8059
Received : , Accepted : , Published Online :