Zimmermann-Laband-1 Syndrome: Clinical, Histological, and Proteomic Findings of a 3-Year-Old Patient with Hereditary Gingival Fibromatosis

Background: Zimmermann-Laband-1 syndrome (ZLS-1; OMIM# 135500) is a rare genetic disorder whose oral pathognomonic sign is the development of progressive, diffuse, and severe gingival hypertrophy. Most children with abnormally gingival hyperplasia may also present multiple unerupted teeth and skelet...

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Detalles Bibliográficos
Autores principales: Guglielmi, Federica, Staderini, Edoardo, Iavarone, Federica, Di Tonno, Laura, Gallenzi, Patrizia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783959/
https://www.ncbi.nlm.nih.gov/pubmed/31261938
http://dx.doi.org/10.3390/biomedicines7030048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783959/
https://www.ncbi.nlm.nih.gov/pubmed/31261938
http://dx.doi.org/10.3390/biomedicines7030048

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