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Omenn's syndrome

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dc.contributor.authorKiliç, Sara Şebnem
dc.contributor.buuauthorKILIÇ GÜLTEKİN, SARA ŞEBNEM
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.contributor.scopusid34975059200
dc.date.accessioned2025-08-07T07:09:30Z
dc.date.issued2003-01-01
dc.description.abstractOmenn's syndrome is characterized by generalized erythematous skin rash, lymph node enlargement, hepatosplenomegaly, increased serum Ig E levels and evidence of combined immune deficiency. We report a two-month-old boy with scaly skin who developed Omenn's syndrome and a review of the literature on this disease.
dc.identifier.endpage42
dc.identifier.issn0885-6265
dc.identifier.issue1
dc.identifier.scopus2-s2.0-0037214917
dc.identifier.startpage41
dc.identifier.urihttps://hdl.handle.net/11452/54345
dc.identifier.volume18
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalInternational Pediatrics
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectOmenn's syndrome
dc.subjectImmunodeficiency
dc.subjectHypogammaglobulinemia
dc.titleOmenn's syndrome
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublicationcb4f5525-5861-44f7-8234-fc2b376a934d
relation.isAuthorOfPublication.latestForDiscoverycb4f5525-5861-44f7-8234-fc2b376a934d

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