Hearing loss in Norwegian adults with achondroplasia

BACKGROUND: Achondroplasia is the most common form of disproportionate skeletal dysplasia. The condition is caused by a mutation in the FGFR3 gene, affecting endochondral bone growth, including the craniofacial anatomy. Recurrent otitis media infections, chronic middle ear effusion, and hearing loss...

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Detalles Bibliográficos
Autores principales: Fredwall, Svein O., Åberg, Björn, Berdal, Hanne, Savarirayan, Ravi, Solheim, Jorunn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570016/
https://www.ncbi.nlm.nih.gov/pubmed/34736503
http://dx.doi.org/10.1186/s13023-021-02095-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570016/
https://www.ncbi.nlm.nih.gov/pubmed/34736503
http://dx.doi.org/10.1186/s13023-021-02095-7

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