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      The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.

      Genetics and molecular research : GMR
      Body Height, genetics, Chromosomes, Human, X, Exons, Female, Humans, Male, Parents, Phenotype, Polymerase Chain Reaction, Receptors, Androgen, Trinucleotide Repeats, Turner Syndrome

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          Abstract

          Thirty-seven 45 X Turner syndrome patients with confirmed peripheral blood lymphocyte karyotype were initially selected to determine the origin of the retained X chromosome and to correlate it with their parents' stature. Blood samples were available in 25 families. The parental origin of the X chromosome was determined in 24 informative families through the analysis of the exon 1-CAG repeat variation of the androgen receptor gene. In 70.8% of the cases, the retained X chromosome was maternal in origin and 29.2% was paternal. When we classified the patients according to maternal (Xm) or paternal (Xp) X chromosome, there was a positive correlation between patients' and maternal heights only in the Xm group. There was no correlation with paternal height in either group, and a significant correlation with target height was only observed in the Xm group. In conclusion, maternal height is the best variable correlating with the height of 45 X Turner syndrome patients who retain the maternal X chromosome, suggesting a strong influence of genes located on the maternal X chromosome on stature.

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