| dc.contributor.author | ÖZGEN, İLKER TOLGA | |
| dc.contributor.author | Yesil, Gözde | |
| dc.contributor.author | CESUR, Yaşar | |
| dc.contributor.author | Kutlu, Esra | |
| dc.date.accessioned | 2021-03-05T11:52:49Z | |
| dc.date.available | 2021-03-05T11:52:49Z | |
| dc.date.issued | 2019 | |
| dc.identifier.citation | ÖZGEN İ. T. , Kutlu E., CESUR Y., Yesil G., "A Case with Laron Syndrome", BEZMIALEM SCIENCE, cilt.7, ss.251-254, 2019 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.other | av_aa5c6569-bb53-4846-94df-bace0f5f38e1 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/113759 | |
| dc.identifier.uri | https://doi.org/10.14235/bas.galenos.2018.2385 | |
| dc.description.abstract | Laron syndrome (LS) is a rare disorder leading to short stature as a result of growth hormone (GH) insensitivity. It is caused by mutations in GH receptor gene and characterized by post-natal growth retardation, craniofacial abnormalities, high serum GH and low insulin-like growth factor-1 (IGF-I) levels. Several different genetic mutations have been documented up to date. In this article, a patient with LS is reported. | |
| dc.language.iso | eng | |
| dc.subject | Klinik Tıp | |
| dc.subject | Klinik Tıp (MED) | |
| dc.subject | Tıp | |
| dc.subject | Sağlık Bilimleri | |
| dc.subject | Temel Tıp Bilimleri | |
| dc.subject | TIP, GENEL & İÇECEK | |
| dc.title | A Case with Laron Syndrome | |
| dc.type | Makale | |
| dc.relation.journal | BEZMIALEM SCIENCE | |
| dc.contributor.department | Bezmiâlem Vakıf Üniversitesi , Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü | |
| dc.identifier.volume | 7 | |
| dc.identifier.issue | 3 | |
| dc.identifier.startpage | 251 | |
| dc.identifier.endpage | 254 | |
| dc.contributor.firstauthorID | 1042664 | |
