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Eur J Med Genet ; 52(4): 207-10, 2009.
Article in English | MEDLINE | ID: mdl-19375526

ABSTRACT

An unusual mosaic karyotype was detected in a 6-year-old female patient with clinical diagnosis of Turner syndrome (TS). Cytogenetic and molecular cytogenetic studies revealed besides a cell line with 45,X a second cell line where the short arm of the Y-chromosome was translocated onto the short arm of a chromosome 7; karyotype: 45,X,der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)/45,X. To delineate the mechanisms of rearrangement and karyotypic evolution in this case, further studies were performed. A maternal origin of the X-chromosome and biparental origin of both chromosomes 7 were determined by microsatellite analysis. Furthermore, using parental-origin-determination fluorescence in situ hybridization (pod-FISH) it could be established that the derivative chromosome 7 was of paternal origin. Overall, this is to the best of our knowledge the first report of such a complex mosaic TS karyotype.


Subject(s)
Chromosomes, Human, Pair 7 , Chromosomes, Human, X , Chromosomes, Human, Y , Mosaicism , Turner Syndrome/genetics , Child , Chromosome Deletion , Fathers , Female , Haplotypes , Humans , In Situ Hybridization, Fluorescence , Karyotyping , Male , Microsatellite Repeats/genetics , Translocation, Genetic , Turner Syndrome/diagnosis
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