Congenital Hypothyroidism With Isolated Fibula Agenesis
dc.authorscopusid | 14526773500 | |
dc.authorscopusid | 8421729700 | |
dc.authorscopusid | 7101974609 | |
dc.authorscopusid | 6603814316 | |
dc.authorscopusid | 6602891195 | |
dc.authorscopusid | 56336609600 | |
dc.authorwosid | Güven, Ahmet/Aaq-6578-2021 | |
dc.authorwosid | Akpınar, Fuat/Gyu-1376-2022 | |
dc.contributor.author | Dogan, Murat | |
dc.contributor.author | Yilmaz, Cahide | |
dc.contributor.author | Caksen, Hueseyin | |
dc.contributor.author | Cesur, Yasar | |
dc.contributor.author | Akpinar, Fuat | |
dc.contributor.author | Gueven, Ahmet Sami | |
dc.date.accessioned | 2025-05-10T17:48:16Z | |
dc.date.available | 2025-05-10T17:48:16Z | |
dc.date.issued | 2010 | |
dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
dc.department-temp | [Dogan, Murat; Cesur, Yasar] Yuzuncu Yil Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Ana Bilim Dali, Cocuk Endokrinol Bilim Dali, Van, Turkey; [Caksen, Hueseyin] Yuzuncu Yil Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Ana Bilim Dali, Cocuk Norol Bilim Dali, Van, Turkey; [Yilmaz, Cahide] Mustafa Kemal Univ, Tip Fak, Cocuk Sagligi & Hastaliklari Ana Bilim Dali, Cocuk Norol Bilim Dali, Antakya, Turkey; [Akpinar, Fuat] Umraniye Egitim & Arastirma Hastanesi, Ortopedi Klin, Istanbul, Turkey; [Gueven, Ahmet Sami] Bayburt Devlet Hastanesi, Cocuk Klin, Bayburt, Turkey | en_US |
dc.description.abstract | Although congenital hypothyroidism is seen often as an isolated case, it can also be seen as a part of some syndromes like Schinzel-Giedion, Aicardi-Goutieres-like, cleidocranial dysplasia and deletion of 18q. It is also well known that congenital hypothyroidism may be associated with other congenital malformations, especially with cardiac heart diseases, skeletal abnormalities, Central nervous system and eye malformations. In this article, 11-years-old-girl with fibula agenesis associated with congenital hypothyroidism because of thyroid gland hypoplasia is presented. In our knowledge, both congenital hypothyroidism and isolated fibula agenesis have not been published before in the literature. | en_US |
dc.description.woscitationindex | Science Citation Index Expanded | |
dc.identifier.endpage | 92 | en_US |
dc.identifier.issn | 1305-2381 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopus | 2-s2.0-77957316057 | |
dc.identifier.scopusquality | Q4 | |
dc.identifier.startpage | 90 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.14720/17027 | |
dc.identifier.volume | 6 | en_US |
dc.identifier.wos | WOS:000281404900017 | |
dc.identifier.wosquality | N/A | |
dc.language.iso | tr | en_US |
dc.publisher | Nobel Ilac | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Congenital Hypothyroidism | en_US |
dc.subject | Isolated Fibula Agenesis | en_US |
dc.subject | Mental Retardation | en_US |
dc.title | Congenital Hypothyroidism With Isolated Fibula Agenesis | en_US |
dc.type | Article | en_US |