Complex characteristics of disorders in Turner syndrome
Khaydarova F.A.Republican Specialized Scientific and Practical Medical Center of Endocrinology of the Ministry of Health of the Republic of Uzbekistan, Tashkent, Republic of UzbekistanKalankhodjayeva Sh.B.Republican Specialized Scientific and Practical Medical Center of Endocrinology of the Ministry of Health of the Republic of Uzbekistan, Tashkent, Republic of Uzbekistan
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Turner syndrome (TS) is a genetic disease associated with the complete or partial loss of one X chromosome, often with a mosaic karyotype. TS is the only one monosomy life-compatible, and affects approximately 1 in 2000-2500-2500 newborn girls [4; 13; 15; 16].
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