A COLLODION BABY WITH HYPOTHYROIDISM
dc.authorid | Dogan, Derya Gumus/0000-0003-1587-9639 | |
dc.authorid | Aslan, Mehmet/0000-0001-5710-6592 | |
dc.authorwosid | Dogan, Derya Gumus/ABG-9945-2020 | |
dc.authorwosid | Aslan, Mehmet/AEL-7823-2022 | |
dc.contributor.author | Dogan, D. G. | |
dc.contributor.author | Aslan, M. | |
dc.contributor.author | Karabiber, H. | |
dc.date.accessioned | 2024-08-04T20:56:15Z | |
dc.date.available | 2024-08-04T20:56:15Z | |
dc.date.issued | 2010 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | A Collodion baby with hypothyroidism: Collodion 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.endpage | 346 | en_US |
dc.identifier.issn | 1015-8146 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 20964127 | en_US |
dc.identifier.startpage | 343 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/102173 | |
dc.identifier.volume | 21 | en_US |
dc.identifier.wos | WOS:000282665700012 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Medecine Et Hygiene | en_US |
dc.relation.ispartof | Genetic Counseling | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Collodion baby | en_US |
dc.subject | Hypothyroidism | en_US |
dc.title | A COLLODION BABY WITH HYPOTHYROIDISM | en_US |
dc.type | Article | en_US |