Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
Makaleler > Tam Makale · 2012
Yazarlar: FATİH GÜRBÜZ, LEMAN DAMLA KOTAN, Eda Mengen, Zeynep Siklar, Merih Berberoglu, Sebila Dokmetas, Mehmet Fatih Kilicli, Ayla Guven, Birgul Kirel, Nurcin Saka, Sukran Poyrazoglu, Yasar Cesur, Murat Dogan, Samim ÖZEN, Mehmet Nuri Ozbek, Huseyin Demirbilek, M. Burcu Kekil, Fatih Temiz, Neslihan Onenli Mungan, Bilgin Yuksel, Ali Kemal Topaloglu
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2012, cilt 4, ss 121-126
DOI: 10.4274/jcrpe.725
Özet
Objective: Normosmic idiopathic hypogonadotropic hypogonadism (nIHH) is characterized by failure of initiation or maintenance of puberty due to insufficient gonadotropin release, which is not associated with anosmia/hyposmia. The objective of this study was to determine the distribution of causative mutations in a hereditary form of nIHH.