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dc.contributor.authorBaltacioglu, Esra
dc.contributor.authorGuzeldemir, Esra
dc.contributor.authorSukuroglu, Erkan
dc.contributor.authorYildiz, Kadriye
dc.contributor.authorYuva, Pinar
dc.contributor.authorAydin, Güven
dc.contributor.authorKaracal, Naci
dc.date.accessioned2019-12-16T06:53:33Z
dc.date.available2019-12-16T06:53:33Z
dc.date.issued2017
dc.identifier.issn0019-5154
dc.identifier.urihttps://doi.org/10.4103/ijd.IJD_166_16
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363149/
dc.identifier.urihttp://hdl.handle.net/11655/19127
dc.description.abstractJuvenile hyaline fibromatosis (JHF) is a rare hereditary disease with an autosomal recessive transmission. JHF is characterized by papulonodular skin lesions, osteolytic bone lesions, flexural joint contractures, and gingival hyperplasia and usually diagnosed in infancy or early childhood. JHF is thought to be a disorder of collagen metabolism and characterized by homogenous amorphous eosinophilic material and fibrous tissue. We report the case of a 14-year-old male child with multiple papulonodular skin lesions, progressive flexion contractures of joints, and severe gingival hyperplasia, with a 10-year follow-up. Although the lesions were totally removed thrice during the last 10 years, they recurred rigorously.
dc.relation.isversionof10.4103/ijd.IJD_166_16
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleJuvenile Hyaline Fibromatosis: A 10-Year Follow-Up
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalIndian Journal of Dermatology
dc.contributor.departmentPeriodontoloji
dc.identifier.volume62
dc.identifier.issue2
dc.identifier.startpage210
dc.identifier.endpage212
dc.description.indexPubMed
dc.description.indexScopus


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