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MON-253 Severe Infantile Hypercalcemia in Williams-Beuren Syndrome

Background: Williams-Beuren Syndrome (WBS) is due to a microdeletion on chromosome 7q11, and is associated with facial dysmorphisms, supravalvular aortic stenosis, a sociable personality and infantile hypercalcemia that is clasically mild and transient. Here we describe an infant found to have incid...

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Detalles Bibliográficos
Autores principales:	Nasir, Hamza, Mucci, Andrea, Rogers, Douglas
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Endocrine Society 2019
Materias:	Pediatric Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551088/ http://dx.doi.org/10.1210/js.2019-MON-253

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