Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the following characteristics: macrosomia, macroglossia, abdominal wall deformities such as omphalocele, visceromegaly, hemihypertrophy and elevated risk of developing tumors such as nephroblastoma or hepatoblastoma. A 2....

Descripción completa

Detalles Bibliográficos
Autores principales: Solanki, Dhruvi, Fulzele, Punit, Bhola, Nitin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pediatric Surgery
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625723/
https://www.ncbi.nlm.nih.gov/pubmed/37933371
http://dx.doi.org/10.7759/cureus.46579

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625723/
https://www.ncbi.nlm.nih.gov/pubmed/37933371
http://dx.doi.org/10.7759/cureus.46579

Ejemplares similares