Investigation of a family affected by early-onset osteoarthritis – proposal of a clinical pathway and bioinformatics pipeline for the investigation of cases of familial OA

BACKGROUND: Familial cases of early-onset osteoarthritis (OA) are rare although the exact prevalence is unknown. Early recognition of underlying OA-associated disorders is vital for targeted treatment, when available, and genetic counselling, in case of skeletal dysplasias. Currently, there is no cl...

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Detalles Bibliográficos
Autores principales: Deveza, Leticia A., Zankl, Andreas, Hunter, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339477/
https://www.ncbi.nlm.nih.gov/pubmed/37443051
http://dx.doi.org/10.1186/s12891-023-06691-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339477/
https://www.ncbi.nlm.nih.gov/pubmed/37443051
http://dx.doi.org/10.1186/s12891-023-06691-5

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