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A Case of Juvenile Crest Syndrome Representing as Failure to Thrive

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dc.contributor.authorOzden, Muge Guler
dc.contributor.authorSaricoban, Hulya Ercan
dc.contributor.authorBuyukgeciz, Benal
dc.date.accessioned2025-12-10T21:39:48Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ozden, Muge Guler] Ondokuz Mayis Univ, Dermatol Anabilim Dali, Samsun, Turkey; [Saricoban, Hulya Ercan; Buyukgeciz, Benal] Yeditepe Univ, Tip Fak, Pediat Bolumu, Istanbul, Turkeyen_US
dc.description.abstractThe CREST syndrome refers to the manifestations of calcinosis, Raynaud's phenomenon, esophageal involvement, sclerodactily and telengiectasisas. Onset during childhood is very uncommon and fewer than 100 cases have been reported in the literature. We describe a 9-year-5 month girl diagnosed as CREST syndrome whose symptoms were present since 1-year-old. Since that time she had been followed as growth failure. This patient points out that growth retardation in childhood may be the initial manifestation of CREST syndrome.en_US
dc.description.woscitationindexEmerging Sources Citation Index
dc.identifier.endpage101en_US
dc.identifier.issn1305-6433
dc.identifier.issn1305-6441
dc.identifier.issue3en_US
dc.identifier.scopusqualityQ4
dc.identifier.startpage99en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34758
dc.identifier.volume72en_US
dc.identifier.wosWOS:000409820800005
dc.language.isoenen_US
dc.publisherIstanbul Univ, Faculty Medicine, Publishing officeen_US
dc.relation.ispartofIstanbul Tip Fakultesi Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA Case of Juvenile Crest Syndrome Representing as Failure to Thriveen_US
dc.typeArticleen_US
dspace.entity.typePublication

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