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PSUN280 A Rare Genetic Disorder With Recurrent Hypoglycemic Episodes and Ketonemia Requiring Multidisciplinary Team Management During Pregnancy

INTRODUCTION: Beckwith-Wiedemann syndrome (BWS; OMIM 130650) is a multisystem human genomic imprinting disorder of chromosome 11p15.5. It is characterized by overgrowth and cancer susceptibility and is known to have a highly variable clinical spectrum. The main features include lateralized overgrowt...

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Detalles Bibliográficos
Autores principales: Nasir, Sadia, Khan, Sidrah, Oyibo, Samson, Lia, Charleen, Greenway, Daisy, Dietician, Specialist
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627651/
http://dx.doi.org/10.1210/jendso/bvac150.840

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