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

Yesilkaya, Ediz; BEREKET, ABDULLAH; Darendeliler, Feyza; Bas, Firdevs; Poyrazoglu, Sukran; Aydin, Banu; DARCAN, ŞÜKRAN; Dundar, Bumin; Buyukinan, Muammer; Kara, Cengiz; Sari, Erkan; Adal, Erdal; AKINCI, AYŞEHAN; ATABEK, MEHMET; Demirel, Fatma; Celik, Nurullah; Ozkan, Behzat; ÖZHAN, BAYRAM; ORBAK, Zerrin; ERSOY, BETÜL; Dogan, Murat; Atas, Ali; DEMİRCİOĞLU, SERAP; Goksen, Damla; Tarim, Omer; YÜKSEL, BİLGİN; Ercan, Oya; Hatun, Sukru; ŞİMŞEK, ENVER; Okten, Aysenur; ABACI, AYHAN; DÖNERAY, Hakan; Ozbek, Mehmet; KESKİN, MEHMET; Onal, Hasan; Akyurek, Nesibe; Bulan, Kezban; Tepe, Derya; Emeksiz, Hamdi; Demir, Korcan; Kizilay, Deniz; TOPALOĞLU, ALİ; EREN, ERDAL; ÖZEN, SAMİM; Abali, Saygin; Akin, Leyla; EKLİOĞLU, BERAY; Kaba, Sultan; Anik, Ahmet; Bas, Serpil; Unuvar, Tolga; Saglam, Halil; Bolu, Semih; Ozgen, Tolga; Dogan, Durmus; Cakir, Esra; ŞEN, YAŞAR; Andiran, Nesibe; Cizmecioglu, Filiz; Evliyaoglu, Olcay; KARAGÜZEL, GÜLAY; Pirgon, Ozgur; Catli, Gonul; Can, Hatice; GÜRBÜZ, FATİH; Binay, Cigdem; Bas, Veysel; Fidanci, Kursat; Polat, Adem; Gul, Davut; Acikel, Cengizhan; Demirbilek, Huseyin; CİNAZ, PEYAMİ; Bondy, Carolyn

doi:10.4274/jcrpe.1771

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

Atıf İçin Kopyala

Yesilkaya E., BEREKET A., Darendeliler F., Bas F., Poyrazoglu S., 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
Çukurova Üniversitesi Adresli: Evet

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.