MON-LB061 Cushing Syndrome Due to an Adrenocortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

Introduction: Beckwith-Wiedemann syndrome (BWS) is a congenital tumor-predisposition syndrome of which around 70% develops because of the methylation defects in the imprinted genes at chromosome 11p15.5. KCNQ1OT1 hypomethylation is the most common underlying genetic aberration in sporadic BWS, accou...

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Detalles Bibliográficos
Autores principales: Bereket, Abdullah, Eltan, Mehmet, Cerit, Kivilcim, Kaygusuz, Sare Betül, Ates, Esra, Ergelen, Rabia, Eker, Nursah, Bagci, Pelin, Turan, Serap, Guran, Tulay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551134/
http://dx.doi.org/10.1210/js.2019-MON-LB061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551134/
http://dx.doi.org/10.1210/js.2019-MON-LB061

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