Artikel ; Online: Heart and Turner syndrome.
2020 Band 82, Heft 3-4, Seite(n) 135–140
Abstract: Turner syndrome (TS) is a rare disease (ORPHA #881) which affects about 50 in 100 000 newborn girls. Their karyotype shows a complete or partial loss of the second X chromosome. In TS, congenital cardiovascular malformations, such as bicuspid aortic ... ...
Abstract | Turner syndrome (TS) is a rare disease (ORPHA #881) which affects about 50 in 100 000 newborn girls. Their karyotype shows a complete or partial loss of the second X chromosome. In TS, congenital cardiovascular malformations, such as bicuspid aortic valves and aortic coarctation are frequent, affecting 20-30% and 7-18% of the TS population, respectively. The morbidity and mortality of these patients are high and related to the presence of hypertension and/or aortic dilatation (40%), inducing aortic dissection. European guidelines published in 2017 have indicated how to monitor patients using magnetic resonance imaging (MRI) and/or echography. Different studies have shown that a cardiovascular lifelong follow-up is necessary and therefore education of patients with TS and their families represents a major issue. This review will present recent data concerning the progression of aortic diameters as well as current molecular knowledge of the cardiovascular system in patients with TS. |
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Mesh-Begriff(e) | Aortic Coarctation/diagnosis ; Aortic Coarctation/epidemiology ; Aortic Coarctation/genetics ; Female ; Heart/physiology ; Humans ; Infant, Newborn ; Magnetic Resonance Imaging ; Turner Syndrome/diagnosis ; Turner Syndrome/epidemiology ; Turner Syndrome/genetics ; Turner Syndrome/physiopathology |
Sprache | Englisch |
Erscheinungsdatum | 2020-12-08 |
Erscheinungsland | France |
Dokumenttyp | Journal Article ; Review |
ZDB-ID | 299-9 |
ISSN | 2213-3941 ; 0003-4266 |
ISSN (online) | 2213-3941 |
ISSN | 0003-4266 |
DOI | 10.1016/j.ando.2020.12.004 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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