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.
Publication date
14/01/2022
Type of Group
Other
Field
Disabilities
Education
Research
Country
Spain
Copy paste the URL
https://www.teaming.net/investigacionsindromedeturner
