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Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome
Hyaline fibromatosis syndrome (HFS) is a rare autosomal recessive genetic disorder characterized by accumulation of hyalinized fibrous tissue with cutaneous, mucosal, osteoarticular, and systemic involvement. The condition is caused by a mutation of ANTXR2 gene that results in a faulty synthesis of...
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| Publicado en: | Acta Stomatol Croat |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
University of Zagreb School of Dental Medicine, and Croatian Dental Society - Croatian Medical Association
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7233120/ https://ncbi.nlm.nih.gov/pubmed/32523159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15644/asc54/1/8 |
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