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Management of airway obstruction in a severe case of juvenile hyaline fibromatosis

dc.contributor.authorKarabulut, AB
dc.contributor.authorDemiryont, M
dc.contributor.authorOnel, D
dc.contributor.authorOzden, BC
dc.date.accessioned2021-03-06T12:44:14Z
dc.date.available2021-03-06T12:44:14Z
dc.date.issued2005
dc.identifier.citationKarabulut A., Ozden B., Onel D., Demiryont M., "Management of airway obstruction in a severe case of juvenile hyaline fibromatosis", ANNALS OF PLASTIC SURGERY, cilt.54, ss.328-330, 2005
dc.identifier.issn0148-7043
dc.identifier.otherav_f54021fb-3426-4be7-9e69-139e26c8c476
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/160751
dc.identifier.urihttps://doi.org/10.1097/01.sap.0000141374.46083.e5
dc.description.abstractJuvenile hyaline fibromatosis (JHF) is an extremely rare, genetic disease with unknown etiology. It is characterized by cutaneous nodules and flexural joint contractures, along with hypertrophy of the gingival and oral mucosa, which is probably the most striking and morbidity-related feature of the disease.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectCERRAHİ
dc.titleManagement of airway obstruction in a severe case of juvenile hyaline fibromatosis
dc.typeMakale
dc.relation.journalANNALS OF PLASTIC SURGERY
dc.contributor.department, ,
dc.identifier.volume54
dc.identifier.issue3
dc.identifier.startpage328
dc.identifier.endpage330
dc.contributor.firstauthorID174556


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