Progressive osseous heteroplasia: A case report with an unexpected trigger

Progressive osseous heteroplasia (POH) is a rare genetic disorder characterised by progressive heterotopic ossification (HO) within the skin and subcutaneous tissues. The condition is caused by heterozygous inactivating mutations of the GNAS gene and usually presents in infancy. We describe the case...

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Detalles Bibliográficos
Autores principales: Boncompagni, Alessandra, Lucas-Herald, Angela K., Beattie, Paula, McDevitt, Helen, Iughetti, Lorenzo, Constantinou, Panayiotis, Kinning, Esther, Ahmed, S. Faisal, Mason, Avril
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015177/
https://www.ncbi.nlm.nih.gov/pubmed/36936194
http://dx.doi.org/10.1016/j.bonr.2023.101665

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015177/
https://www.ncbi.nlm.nih.gov/pubmed/36936194
http://dx.doi.org/10.1016/j.bonr.2023.101665

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