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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, Yaşar
dc.contributor.authorAkpinar, Fuat
dc.contributor.authorGueven, Ahmet Sami
dc.contributor.institutionauthorCESUR, YAŞAR
dc.date.accessioned2020-10-21T20:21:31Z
dc.date.available2020-10-21T20:21:31Z
dc.date.issued2010-05-01T00:00:00Z
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.
dc.identifier.citationDogan M., Yilmaz C., Caksen H., Cesur Y., Akpinar F., Gueven A. S. , -CONGENITAL HYPOTHYROIDISM WITH ISOLATED FIBULA AGENESIS-, NOBEL MEDICUS, cilt.6, ss.90-92, 2010
dc.identifier.scopus77957316057
dc.identifier.trdizintrdizin
dc.identifier.urihttp://hdl.handle.net/20.500.12645/23416
dc.identifier.wosWOS:000281404900017
dc.titleCONGENITAL HYPOTHYROIDISM WITH ISOLATED FIBULA AGENESIS
dc.typeArticle
dspace.entity.typePublication
local.avesis.id13f4cd1f-f001-437c-81d3-a906e7188995
local.publication.isinternational1
relation.isAuthorOfPublicationddd881a5-c7cb-41e5-b4e1-0693a98a0d29
relation.isAuthorOfPublication.latestForDiscoveryddd881a5-c7cb-41e5-b4e1-0693a98a0d29
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