Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study

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dc.authorid243608)en_US
dc.authorid9240en_US
dc.authorid7445en_US
dc.authorid107300en_US
dc.contributor.authorYeşilkaya, Ediz
dc.contributor.authorBereket, Abdullah
dc.contributor.authorDarendeliler, Feyza
dc.contributor.authorBaş, Firdevs
dc.date.accessioned2017-07-09T08:53:15Z
dc.date.available2017-07-09T08:53:15Z
dc.date.issued2015
dc.departmentİnönü Üniversitesien_US
dc.descriptionJ Clin Res Pediatr Endocrinol 2015;7(1):27-36en_US
dc.description.abstractTurner syndrome (TS) is a genetic disorder characterized by total or partial absence of one sex chromosome (1). It is one of the most common chromosomal disorder with an incidence of 1:2500 female live births (2,3). The most prevalent karyotype is 45,X, followed by mosaic patterns. TS is associated with several morbidities that increase with age. Although TS causes several multisystem disorders, the most common presentation is usually due to short stature and primary gonadal deficiency. Patients may present with congenital malformations such as horseshoe kidney and coarctation of the aorta. They may also develop diabetes, hypothyroidism, hypertension, hearing loss, osteoporosis and bone fractures (4,5). Timely diagnosis and proper management of associated problems may reduce substantial morbidity and mortality and improve the quality of life in TS patients. Studies based on a large pediatric population which provide data on frequency of associated problems and their distribution among the different karyotypes are scarce (6,7,8). In the present study, we aimed to define the frequency of associated problems in TS patients during childhood and the distribution of these clinical features according to karyotype and age by evaluating 842 patients with TS from 35 centers in Turkeyen_US
dc.identifier.citationEDİZ, Y., BEREKET, A., DARENDELİLER, F. F., BAŞ, F., POYRAZOĞLU, Ş., BANU, K., … AKINCI, A. (2015). Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study. Journal of Clinical Research in Pediatric Endocrinology, 7(1), 27–36.en_US
dc.identifier.doi10.4274/jcrpe.1771en_US
dc.identifier.endpage36en_US
dc.identifier.issue1en_US
dc.identifier.startpage27en_US
dc.identifier.urihttp://cms.galenos.com.tr/FileIssue/1/793/article/27-36.pdf
dc.identifier.urihttps://hdl.handle.net/11616/7325
dc.identifier.volume7en_US
dc.language.isoenen_US
dc.publisherJournal of Clinical Research in Pediatric Endocrinologyen_US
dc.relation.ispartofJournal of Clinical Research in Pediatric Endocrinologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectNationwide studyen_US
dc.subjectTurner syndromeen_US
dc.subjectChildrenen_US
dc.subjectDiagnostic featuresen_US
dc.subjectAssociated problemsen_US
dc.titleTurner Syndrome and Associated Problems in Turkish Children A Multicenter Studyen_US
dc.typeArticleen_US

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