1. A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype
- Author
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Yusuf Ozkul, M. Emre Atabek, Cetin Saatci, Selim Kurtoglu, and Munis Dundar
- Subjects
Genetics ,Turner Syndrome ,High resolution ,Karyotype ,Anatomy ,Biology ,Chromosomal anomaly ,medicine.disease ,Translocation, Genetic ,Chromosomes, Human, Pair 1 ,Chromosomes, Human, Pair 2 ,Karyotyping ,Turner syndrome ,medicine ,Humans ,Female ,Anomaly (physics) ,Child - Abstract
The most common chromosomal anomaly is 45,X in the Turner syndrome. In addition to this, anomaly, mosaicism such as structural 46,X,i(Xq), 46,X,del(Xp), 46,X,r(X), 46,X,t(X;Y) and numerical 46XO/46,XX/47XXX are seen rather frequently. An infant with the Turner syndrome was found to have a karyotype 45X,t(1;2) (q41;p16) using high resolution banding. Based on our knowledge, we present the first case of 45X,t(1;2) (q41;p11.2), a karyotype in Turner's syndrome in the literature. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
- Published
- 2002
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