Recurrent Hypoglycemia Secondary to Insulinoma in an Adult With Beckwith-Wiedemann Syndrome

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder characterized by genetic and epigenetic changes on the chromosome 11p15.5 region, which includes genes that are important for fetal and postnatal growth. Children with BWS have a higher chance of having hypoglycemia, hyperinsulinemia, and...

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Detalles Bibliográficos
Autores principales: Akcan, Tugce, Shariff, Julia Rose R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580426/
https://www.ncbi.nlm.nih.gov/pubmed/37908580
http://dx.doi.org/10.1210/jcemcr/luad062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580426/
https://www.ncbi.nlm.nih.gov/pubmed/37908580
http://dx.doi.org/10.1210/jcemcr/luad062

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