Abstract
All of us know that Turner Syndrome (TS) is a congenital disease caused by a complete or partial loss of one of sex chromosome, which occur in 1:2500 female lives births [ [1] Corbitt H. Gutierrez J. Silberbach M. Maslen Ch The genetic basis of Turner syndrome aortopathy. Am J Med Genet C Semin Med Genet. 2019 March; 117–125 Google Scholar ]. The major phenotypic characteristics of these girls are: 1.Short stature. 2.Gonadal dysgenesis. 3.Congenital anomalies. 4.Neurocognitive problems.
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