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

Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseus 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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Bibliographic Details
Main Authors: Antonio José Justicia-Grande, Jose Gómez-Ríal, Irene Rivero-Calle, Sara Pischedda, María José Curras-Tuala, Alberto Gómez-Carballa, Miriam Cebey-López, Jacobo Pardo-Seco, Roberto Méndez-Gallart, María José Fernández-Seara, Antonio Salas, Federico Martinón-Torres
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Pediatrics
Subjects:
progressive osseous heteroplasia
POH
treatment
genetic diseases
monochorionic twins
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.662669/full

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https://www.frontiersin.org/articles/10.3389/fped.2021.662669/full

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