Abnormal eruption of teeth in relation to FGFR1 heterozygote mutation: a rare case of osteoglophonic dysplasia with 4-year follow-up

BACKGROUND: We report a case and its 4-year follow-up of Osteoglophonic dysplasia (OD), a rare disease that disturbs both skeletal and dental development, which is usually caused by heterozygous FGFR1 mutations. CASE PRESENTATION: This article presents a case where a 6-year-old male patient suffered...

Descripción completa

Detalles Bibliográficos
Autores principales: Zou, Yuchun, Lin, Hanyu, Chen, Weijia, Chang, Lin, Cai, Senxin, Lu, You-Guang, Xu, Linyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832749/
https://www.ncbi.nlm.nih.gov/pubmed/35148738
http://dx.doi.org/10.1186/s12903-022-02069-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832749/
https://www.ncbi.nlm.nih.gov/pubmed/35148738
http://dx.doi.org/10.1186/s12903-022-02069-6

Ejemplares similares