CONGENITAL HYPOTHYROIDISM WITH ISOLATED FIBULA AGENESIS

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dc.contributor.authorDogan, Murat
dc.contributor.authorYilmaz, Cahide
dc.contributor.authorCaksen, Hueseyin
dc.contributor.authorCesur, Yasar
dc.contributor.authorAkpinar, Fuat
dc.contributor.authorGueven, Ahmet Sami
dc.date.accessioned2024-09-18T20:11:47Z
dc.date.available2024-09-18T20:11:47Z
dc.date.issued2010
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractAlthough 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.identifier.endpage92en_US
dc.identifier.issn1305-2381
dc.identifier.issue2en_US
dc.identifier.startpage90en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/9068
dc.identifier.volume6en_US
dc.identifier.wosWOS:000281404900017en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherNobel Ilacen_US
dc.relation.ispartofNobel Medicusen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital hypothyroidismen_US
dc.subjectisolated fibula agenesisen_US
dc.subjectmental retardationen_US
dc.titleCONGENITAL HYPOTHYROIDISM WITH ISOLATED FIBULA AGENESISen_US
dc.typeArticleen_US

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