A Collodion baby with hypothyroidism

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dc.authorscopusid6603090287
dc.authorscopusid57197007210
dc.authorscopusid6701425167
dc.contributor.authorDogan D.G.
dc.contributor.authorAslan M.
dc.contributor.authorKarabiber H.
dc.date.accessioned2024-08-04T19:59:40Z
dc.date.available2024-08-04T19:59:40Z
dc.date.issued2010
dc.departmentİnönü Üniversitesien_US
dc.description.abstractCollodion baby is a rare keratinizing congenital disorder. Although it is milder in degree than harlequin fetus, the infant is at risk for increased water loss, thermal instability, percutaneous toxicity, and infection as a result of an impaired skin barrier function. Here we report on an 11 days-old collodion baby with hypernatremic dehydratation, septicemia and congenital hypothyroidism. To our knowledge congenital hypothyroidism associated with collodion baby is reported in only one case up to date.en_US
dc.identifier.endpage346en_US
dc.identifier.issn1015-8146
dc.identifier.issue3en_US
dc.identifier.pmid20964127en_US
dc.identifier.scopus2-s2.0-77957740487en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage343en_US
dc.identifier.urihttps://hdl.handle.net/11616/90808
dc.identifier.volume21en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCollodion babyen_US
dc.subjectHypothyroidismen_US
dc.titleA Collodion baby with hypothyroidismen_US
dc.typeArticleen_US

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