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Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseous Heteroplasia

Progressive osseous heteroplasia (POH; OMIM 166350) is a rare autosomal-dominant genetic disorder in which extra-skeletal bone forms within skin and muscle tissue. POH is one of the clinical manifestations of an inactivating mutation in the GNAS gene. GNAS gene alterations are difficult matter to ad...

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Detalles Bibliográficos
Autores principales:	Justicia-Grande, Antonio José, Gómez-Ríal, Jose, Rivero-Calle, Irene, Pischedda, Sara, Curras-Tuala, María José, Gómez-Carballa, Alberto, Cebey-López, Miriam, Pardo-Seco, Jacobo, Méndez-Gallart, Roberto, Fernández-Seara, María José, Salas, Antonio, Martinón-Torres, Federico
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8260848/ https://www.ncbi.nlm.nih.gov/pubmed/34249809 http://dx.doi.org/10.3389/fped.2021.662669

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