Evaluation of Two Cases With 45,1 / 46,X, i(Xq) and 46,X, i(Xq) Karyotypes

AYNUR ACAR, TÜLİN ÇORA, HASAN ACAR, Sennur Demirel, İbrahim Erkul, Said Gönen

  • Year : 1990
  • Vol : 6
  • Issue : 3
  •  Page : 315-319
A 12 years old fernak case who was one of the twin sisters and the other 20 years old female case with growth deficiency and lack of menstrual period were referred to our laboratory for possible Turner Syndrome. The first case whose twin sister had normal growth and development with 46, XX karyotype, had a karyotype of 45,X146,X,i (Xq). The karyotype of second female case was 46,X,i (Xq). Cytogenetical findings evaluated together with their cilinical features enabled to distinguish structural anomaly of X chromosomes from the classical 45X Turner syndrome, and the importance of the correlation of phenotype to karyotype is discussed in this article
Cite this Article As :
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.
Evaluation of Two Cases With 45,1 / 46,X, i(Xq) and 46,X, i(Xq) Karyotypes
, Vol. 6 (3)
Received : 18.11.1990, Accepted : 18.11.1990, Published Online : 18.11.2020
Selçuk Tıp Dergisi
ISSN:1017-6616;
E-ISSN:2149-8059;