Синдром дисгенезии гонад (тип Шерешевского-Тернера) у ребёнка раннего возраста

The syndrome Shereshevsky-Turner is genetically determined disease and there is frequency 1 case on 2000-2500 girls born by the live. For the given pathology the triad of signs is characteristic: low growth, gonad's dysgenesis and congenital anomalies of various bodies. Chromosomal anomalies at the given syndrome are shown in the form of absence of one of two chromosomes Х: deletion parts of one chromosome Х, also are possible various mosaic variants when the chromosomal complement is partially kept. Diagnosis of Shereshevsky-Turner syndrome is established only on the basis of cariotype's research. The primary goals of treatment of patients with Shereshevsky-Turner syndrome at children's and teenage age is the following: Increase in final growth, Formation of secondary sexual signs and an establishment of the regular menstrual cycle, Correction of developmental anomalies, treatment of accompanying diseases, Osteoporosis preventive maintenance.