Síndrome de Beckwith Wiedemann

Authors

  • Dania Faxas Rodríguez
  • Ramón Varela González
  • Laidenis Pascual Carreño
  • Yanelis Inés Infante López
  • Gelenis Puig Pérez

Keywords:

MACROSOMÍA FETAL, HERNIA UMBILICAL, MACROGLOSSIA.

Abstract

Se presenta el caso de un paciente, atendido en el Servicio de Pediatría del Hospital General Docente “14 de Junio” del municipio de Jobabo, provincia de Las Tunas. El paciente es portador de un síndrome de Beckwith Wiedemann, enfermedad de posible origen genético autosómico dominante, cuyo diagnóstico se fundamenta en criterios clínicos mayores y menores. Se expusieron los resultados del examen clínico y de las investigaciones complementarias. Se realizó una revisión de la literatura médica sobre el tema.

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Author Biography

Dania Faxas Rodríguez

 

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Published

2015-12-17

How to Cite

1.
Faxas Rodríguez D, Varela González R, Pascual Carreño L, Infante López YI, Puig Pérez G. Síndrome de Beckwith Wiedemann. Rev. electron. Zoilo [Internet]. 2015 Dec. 17 [cited 2025 Oct. 11];38(3). Available from: https://revzoilomarinello.sld.cu/index.php/zmv/article/view/581

Issue

Vol. 38 No. 3 (2013): March

Section

Case reports

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