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Diagnosis and Management of Beckwith-Wiedemann Syndrome

Beckwith-Wiedemann syndrome (BWS) is a human genomic imprinting disorder that presents with a wide spectrum of clinical features including overgrowth, abdominal wall defects, macroglossia, neonatal hypoglycemia, and predisposition to embryonal tumors. It is associated with genetic and epigenetic cha...

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Detalles Bibliográficos
Autores principales:	Wang, Kathleen H., Kupa, Jonida, Duffy, Kelly A., Kalish, Jennifer M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6990127/ https://www.ncbi.nlm.nih.gov/pubmed/32039119 http://dx.doi.org/10.3389/fped.2019.00562

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