Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

OBJECTIVE: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls. This study aimed to systematically investigate the key clinical features...

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Detalles Bibliográficos
Autores principales: Yeşilkaya, Ediz, Bereket, Abdullah, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Küçükemre Aydın, Banu, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Sarı, Erkan, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat, Ataş, Ali, Turan, Serap, Gökşen, Damla, Tarım, Ömer, Yüksel, Bilgin, Ercan, Oya, Hatun, Şükrü, Şimşek, Enver, Ökten, Ayşenur, Abacı, Ayhan, Döneray, Hakan, Özbek, Mehmet Nuri, Keskin, Mehmet, Önal, Hasan, Akyürek, Nesibe, Bulan, Kezban, Tepe, Derya, Emeksiz, Hamdi Cihan, Demir, Korcan, Kızılay, Deniz, Topaloğlu, Ali Kemal, Eren, Erdal, Özen, Samim, Abalı, Saygın, Akın, Leyla, Selver Eklioğlu, Beray, Kaba, Sultan, Anık, Ahmet, Baş, Serpil, Ünüvar, Tolga, Sağlam, Halil, Bolu, Semih, Özgen, Tolga, Doğan, Durmuş, Çakır, Esra Deniz, Şen, Yaşar, Andıran, Nesibe, Çizmecioğlu, Filiz, Evliyaoğlu, Olcay, Karagüzel, Gülay, Pirgon, Özgür, Çatlı, Gönül, Can, Hatice Dilek, Gürbüz, Fatih, Binay, Çiğdem, Baş, Veysel Nijat, Fidancı, Kürşat, Polat, Adem, Gül, Davut, Açıkel, Cengizhan, Demirbilek, Hüseyin, Cinaz, Peyami, Bondy, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439889/
https://www.ncbi.nlm.nih.gov/pubmed/25800473
http://dx.doi.org/10.4274/jcrpe.1771

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439889/
https://www.ncbi.nlm.nih.gov/pubmed/25800473
http://dx.doi.org/10.4274/jcrpe.1771

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