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

Yesilkaya, Ediz; BEREKET, ABDULLAH; DARENDELİLER, Fatma; BAŞ, Firdevs; POYRAZOĞLU, Şükran; Aydin, Banu; DARCAN, ŞÜKRAN; Dundar, Bumin; Buyukinan, Muammer; Kara, Cengiz; Sari, Erkan; Adal, Erdal; Akinci, Aysehan; Atabek, Mehmet; Demirel, Fatma; Celik, Nurullah; Ozkan, Behzat; Ozhan, Bayram; Orbak, Zerrin; Ersoy, Betul; Dogan, Murat; Atas, Ali; Turan, Serap; Goksen, Damla; Tarim, Omer; Yuksel, Bilgin; Ercan, Oya; Hatun, Sukru; Simsek, Enver; Okten, Aysenur; Abaci, Ayhan; Doneray, Hakan; Ozbek, Mehmet; Keskin, Mehmet; Onal, Hasan; Akyurek, Nesibe; Bulan, Kezban; Tepe, Derya; Emeksiz, Hamdi; Demir, Korcan; Kizilay, Deniz; Topaloglu, Ali; Eren, Erdal; Ozen, Samim; Abali, Saygin; Akin, Leyla; Eklioglu, Beray; Kaba, Sultan; Anik, Ahmet; Bas, Serpil; Unuvar, Tolga; Saglam, Halil; Bolu, Semih; Ozgen, Tolga; Dogan, DURMUŞ; Cakir, Esra; Sen, Yasar; Andiran, Nesibe; Cizmecioglu, Filiz; Evliyaoglu, Olcay; Karaguzel, Gulay; Pirgon, Ozgur; Catli, Gonul; Can, Hatice; Gurbuz, Fatih; Binay, Cigdem; Bas, Veysel; Fidanci, Kursat; Polat, Adem; Gul, Davut; Acikel, Cengizhan; Demirbilek, Huseyin; Cinaz, Peyami; Bondy, Carolyn

doi:10.4274/jcrpe.1771

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

Yesilkaya E., BEREKET A., DARENDELİLER F. F., BAŞ F., POYRAZOĞLU Ş., Aydin B. K., ...Daha Fazla

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 7 Sayı: 1
Basım Tarihi: 2015
Doi Numarası: 10.4274/jcrpe.1771
Dergi Adı: JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
Sayfa Sayıları: ss.27-36
Çanakkale Onsekiz Mart Üniversitesi Adresli: Hayır

Özet

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.