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A Case with Laron Syndrome

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dc.contributor.authorÖZGEN, İLKER TOLGA
dc.contributor.authorCESUR, Yaşar
dc.contributor.authorKutlu, Esra
dc.contributor.authorYesil, Gozde
dc.contributor.institutionauthorÖZGEN, İLKER TOLGA
dc.contributor.institutionauthorKUTLU, ESRA
dc.contributor.institutionauthorCESUR, YAŞAR
dc.contributor.institutionauthorYEŞİL, GÖZDE
dc.date.accessioned2020-04-03T20:59:27Z
dc.date.available2020-04-03T20:59:27Z
dc.date.issued2019-07-01T00:00:00Z
dc.description.abstractLaron 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.identifier.citationÖZGEN İ. T. , Kutlu E., CESUR Y., Yesil G., -A Case with Laron Syndrome-, BEZMIALEM SCIENCE, cilt.7, ss.251-254, 2019
dc.identifier.doi10.14235/bas.galenos.2018.2385
dc.identifier.scopus85066857268
dc.identifier.urihttps://hdl.handle.net/20.500.12645/16237
dc.identifier.wosWOS:000499482100015
dc.language.isoen
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleA Case with Laron Syndrome
dc.typeArticle
dspace.entity.typePublication
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local.publication.isinternational1
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relation.isAuthorOfPublication.latestForDiscoveryd38d4d40-416b-4896-af90-986085241849
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