Juvenile hyaline fibromatosis: a rare oral disease case report and literature review

Juvenile hyaline fibromatosis (JHF) is a rare recessive autosomal hereditary disorder characterized by papulonodular skin, gingival hyperplasia, flexural joint contractures, and osteolytic bone lesions. Worldwide, less than 70 cases have been reported. JHF is thought to be a disorder of collagen met...

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Detalles Bibliográficos
Autores principales: Xia, Liang, Hu, Yuhua, Zhang, Chunye, Wu, Dandan, Chen, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649598/
https://www.ncbi.nlm.nih.gov/pubmed/34976780
http://dx.doi.org/10.21037/tp-21-169

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649598/
https://www.ncbi.nlm.nih.gov/pubmed/34976780
http://dx.doi.org/10.21037/tp-21-169

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