| Literature DB >> 19514616 |
M Berková1, Z Berka, Z Krcová.
Abstract
Turner syndrome is one of the most frequent genetic disorders, the result of complete or partial monosomy of the X chromosome. It affects 1 : 2,500 live female births. The principal features of Turner syndrome are short stature and ovarian dysgenesis accompanied by estrogen deficit. Turner syndrome is associated with further numerous, more or less serious abnormalities and high risk of cardiovascular mortality. The article concisely summarizes the most frequent problems in Turner syndrome and emphasizes the need of multidisciplinary care for affected patients.Entities:
Mesh:
Year: 2009 PMID: 19514616
Source DB: PubMed Journal: Vnitr Lek ISSN: 0042-773X