Resumo

BULLER VIQUEIRA, Eva; UREBA RUBIO, Rosalía  e  CABELLO PULIDO, Juana. Beckwith-Wiedemann Syndrome. Rev Clin Med Fam [online]. 2014, vol.7, n.1, pp.66-68. ISSN 2386-8201.  https://dx.doi.org/10.4321/S1699-695X2014000100012.

Beckwith-Wiedemann Syndrome (BWS) is a congenital multisystemic syndrome characterized by hypoglycemia and macrosomia, being the most common macroglossia, high weight at birth, omphalocele and visceromegaly. The present is the case of a five year-old girl with BWS who comes to the healthcare center to follow up of her pathology.

Palavras-chave : Beckwith-Wiedemann syndrome; Macroglossia; Gigantism.

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