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

Date
2015
Author
Goksen, Damla
Eklioglu, Beray Selver
Kaba, Sultan
Anik, Ahmet
Bas, Serpil
UNUVAR, Tolga
Saglam, Halil
Bolu, Semih
OZGEN, Tolga
Dogan, Durmus
Cakir, Esra Deniz
Sen, Yasar
Andiran, Nesibe
Cizmecioglu, Filiz
Karaguzel, Gulay
Pirgon, Ozgur
Catli, Gonul
Can, Hatice Dilek
Gurbuz, Fatih
Binay, Cigdem
BAS, Veysel Nijat
FIDANCI, Kursat
POLAT, Adem
GUL, Davut
ACIKEL, Cengizhan
DEMIRBILEK, Huseyin
Cinaz, Peyami
BONDY, Carolyn
Ercan, Oya
Evliyaoglu, Olcay
Darendeliler, Fatma Feyza
Poyrazoglu, Sukran
Bas, Firdevs
YESILKAYA, Ediz
BEREKET, ABDULLAH
Aydin, Banu Kucukemre
DARCAN, ŞÜKRAN
Dundar, Bumin
BUYUKINAN, Muammer
Kara, Cengiz
SARI, Erkan
ADAL, Erdal
Akinci, Aysehan
Atabek, Mehmet Emre
Demirel, Fatma
Celik, Nurullah
OZKAN, Behzat
Ozhan, Bayram
Orbak, Zerrin
Ersoy, Betul
Dogan, Murat
Atas, Ali
Turan, Serap
Tarim, Omer
Yuksel, Bilgin
Hatun, Sukru
Simsek, Enver
Okten, Aysenur
Abaci, Ayhan
Doneray, Hakan
OZBEK, Mehmet Nuri
Keskin, Mehmet
ONAL, Hasan
Akyurek, Nesibe
Bulan, Kezban
Tepe, Derya
Emeksiz, Hamdi Cihan
DEMIR, Korcan
Kizilay, Deniz
Topaloglu, Ali Kemal
Eren, Erdal
Ozen, Samim
Abali, Saygin
AKIN, Leyla
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Abstract
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 of TS in relationship to karyotype in a large pediatric Turkish patient population.
URI
http://hdl.handle.net/20.500.12627/98234
https://doi.org/10.4274/jcrpe.1771
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