Cargando…
A novel nonsense PTH1R variant shows incomplete penetrance of primary failure of eruption: a case report
BACKGROUND: Aim of this work was to describe a rare inheritance pattern of Primary Failure of Eruption (PFE) in a small family with incomplete penetrance of PFE and a novel nonsense PTH1R variant. CASE PRESENTATION: The proband, a 26 year-old man with a significant bilateral open-bite, was diagnosed...
Autores principales: | Grippaudo, Cristina, Cafiero, Concetta, D’Apolito, Isabella, Re, Agnese, Genuardi, Maurizio, Chiurazzi, Pietro, Frazier-Bowers, Sylvia A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858648/ https://www.ncbi.nlm.nih.gov/pubmed/31730001 http://dx.doi.org/10.1186/s12903-019-0944-9 |
Ejemplares similares
-
Validating clinical characteristics of primary failure of eruption (PFE) associated with PTH1R variants
por: Grippaudo, Cristina, et al.
Publicado: (2021) -
Exfoliative Cytology and Genetic Analysis for a Non-Invasive Approach to the Diagnosis of White Sponge Nevus: Case Series
por: Lajolo, Carlo, et al.
Publicado: (2023) -
Optimization of DNA extraction from dental remains
por: Cafiero, Concetta, et al.
Publicado: (2019) -
A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance
por: Kurban, Mazen, et al.
Publicado: (2011) -
Identification of a novel PTH1R variant in a family with primary failure of eruption
por: Zha, Yunchen, et al.
Publicado: (2023)