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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Detalhes bibliográficos
Publicado no:Front Pediatr
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Pediatrics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8260848/
https://ncbi.nlm.nih.gov/pubmed/34249809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2021.662669
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