Do you know this syndrome? Werner syndrome

dc.contributor.authorBilgic, Ozlem
dc.date.accessioned2020-03-26T19:34:57Z
dc.date.available2020-03-26T19:34:57Z
dc.date.issued2017
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractWerner syndrome is a rare autosomal recessive disorder, caused by mutations in the WRN gene. Clinical findings include: senile appearance, short stature, grey hair, alopecia, bird-like face, scleroderma-like skin changes, skin ulcers, voice abnormalities, cataracts, osteoporosis, type 2 diabetes mellitus, ischemic heart disease and hypogonadism. The syndrome begins to become apparent in adolescence but it is usually diagnosed in the third or fourth decade of life. Since the patients usually die by the age of 40-50 years related to malignant neoplasms or atherosclerotic complications, they should be closely followed and treated for complications.en_US
dc.identifier.doi10.1590/abd1806-4841.20174640en_US
dc.identifier.endpage268en_US
dc.identifier.issn0365-0596en_US
dc.identifier.issn1806-4841en_US
dc.identifier.issue2en_US
dc.identifier.pmid28538897en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage267en_US
dc.identifier.urihttps://dx.doi.org/10.1590/abd1806-4841.20174640
dc.identifier.urihttps://hdl.handle.net/20.500.12395/34979
dc.identifier.volume92en_US
dc.identifier.wosWOS:000401984800026en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSOC BRASILEIRA DERMATOLOGIAen_US
dc.relation.ispartofANAIS BRASILEIROS DE DERMATOLOGIAen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectLeg ulceren_US
dc.subjectProgeriaen_US
dc.subjectScleroderma, localizeden_US
dc.subjectWerner syndromeen_US
dc.titleDo you know this syndrome? Werner syndromeen_US
dc.typeEditorialen_US

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