Turner syndrome (TS) (ORPHA:881, ICD-10: Q96) is a chromosomal disorder characterized by the total absence (pure 45XO karyotype) or partial absence of the X chromosome (mosaic karyotype) with a prevalence of 1:5000 live births ( 1:2500 female births). The clinical findings of the syndrome are heterogeneous and the phenotype is usually mild or absent. Research is essential to better know and understand TS.
Datum der Veröffentlichung
14/01/2022
Art der Gruppe
Andere
Feld
Behinderung
Forschung
Schule und Ausbildung
Land
Spanien
Kopiere die URL und füge sie ein
https://www.teaming.net/investigacionsindromedeturner
