Mazabraud's syndrome: A case report supported by molecular studies and review of the literature

Mazabraud's syndrome represents rare benign disorder characterized by simultaneous occurrence of fibrous dysplasia of bone and intramuscular myxomas within surrounding soft tissue. Mutations of GNAS1 gene were proven to be causative for this condition. Here, we present a case report of a patien...

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Detalles Bibliográficos
Autores principales: Kašpar, Ludvík, Balko, Jan, Strnadová, Martina, Krsková, Lenka, Máška, David, Zámečník, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220459/
https://www.ncbi.nlm.nih.gov/pubmed/37250204
http://dx.doi.org/10.1016/j.bonr.2023.101685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220459/
https://www.ncbi.nlm.nih.gov/pubmed/37250204
http://dx.doi.org/10.1016/j.bonr.2023.101685

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