Publication: Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome
dc.contributor.author | Sanal, Özden | |
dc.contributor.author | Tezcan, İlhan | |
dc.contributor.author | Ersoy, Figen | |
dc.contributor.buuauthor | Kılıç, Sara Şebnem | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Pediatri Bölümü | |
dc.contributor.scopusid | 34975059200 | |
dc.date.accessioned | 2022-01-21T07:42:25Z | |
dc.date.available | 2022-01-21T07:42:25Z | |
dc.date.issued | 2002 | |
dc.description.abstract | Hyperimmunoglobulin E syndrome (hyper-IgE) is a rare immunodeficiency disease associated with recurrent pyogenic infections, chronic eczematoid dermatitis and osteopenia. We present here a 13-year-old girl with hyperimmunoglobulin E syndrome, who developed osteochondritis dissecans (OCD) of the lateral femoral condyle, which is rare. Osteopenia, which is frequently associated with hyper IgE, may predispose the patient to the development of OCD. | |
dc.identifier.citation | Kılıç, S. S. vd. (2002). "Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome". Turkish Journal of Pediatrics, 44(4), 357-359. | |
dc.identifier.endpage | 359 | |
dc.identifier.issn | 0041-4301 | |
dc.identifier.issue | 4 | |
dc.identifier.pubmed | 12458817 | |
dc.identifier.scopus | 2-s2.0-0036807296 | |
dc.identifier.startpage | 357 | |
dc.identifier.uri | http://hdl.handle.net/11452/24208 | |
dc.identifier.volume | 44 | |
dc.identifier.wos | 000179136500018 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Türkiye Milli Pediatri Derneği | |
dc.relation.collaboration | Yurt içi | |
dc.relation.journal | Turkish Journal of Pediatrics | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Bone abnormalities | |
dc.subject | Hyperimmunoglobulin E syndrome | |
dc.subject | Osteochondritis dissecans | |
dc.subject | Osteopenia | |
dc.subject.emtree | Adolescent | |
dc.subject.emtree | Article | |
dc.subject.emtree | Dermatitis | |
dc.subject.emtree | Case report | |
dc.subject.emtree | Disease predisposition | |
dc.subject.emtree | Eczema | |
dc.subject.emtree | Female | |
dc.subject.emtree | Femur condyle | |
dc.subject.emtree | Human | |
dc.subject.emtree | Hyperimmunoglobulinemia E | |
dc.subject.emtree | Immune deficiency | |
dc.subject.emtree | Osteochondritis dissecans | |
dc.subject.emtree | Osteopenia | |
dc.subject.emtree | Recurrent infection | |
dc.subject.mesh | Adolescent | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Job's syndrome | |
dc.subject.mesh | Knee joint | |
dc.subject.mesh | Osteochondritis dissecans | |
dc.subject.scopus | Job Syndrome; Mucocutaneous Candidiasis; Gain of Function Mutation | |
dc.subject.wos | Pediatrics | |
dc.title | Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome | |
dc.type | Article | |
dc.wos.quartile | Q4 | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Pediatri Bölümü | |
local.indexed.at | Scopus | |
local.indexed.at | WOS |