Incomplete Moebius syndrome. Clinical case presentation

Authors

  • Damarys Hernández Suárez Universidad de Ciencias Médicas de Matanzas. Matanzas.
  • María Elena Blanco Pereira Universidad de Ciencias Médicas de Matanzas. Matanzas.
  • Elsa Juana Luna Ceballos Universidad de Ciencias Médicas de Matanzas. Matanzas.
  • Grecia Martínez Leyva Universidad de Ciencias Médicas de Matanzas. Matanzas.
  • Dalmara Hernández Suárez Universidad de Ciencias Médicas de Matanzas. Matanzas.
  • Aralys Peréz García Universidad de Ciencias Médicas de Matanzas. Matanzas.

Keywords:

Moebius syndrome, congenital facial paralysis, congenital paralysis of the VI and VII cranial nerves nuclei.

Abstract

Moebius syndrome is a non-progressive poli-formative disorder characterized by facial congenital paralysis. It is defined as a congenital paralysis of the VI and VII cranial nerves nuclei, the clinical spectrum of which is variable and associated to several bone and muscular malformations. It is few frequent and has vascular, genetic or multifactorial etiology. This work, based on more updated theoretical fundaments, pretended to describe the clinical manifestations of the Moebius syndrome and its possible etiology on the purpose of a case. It is the case of a patient, aged 11 years, who presented facial asymmetry, lips commissure deviation to the left, semi-opened mouth, constant lagrimeo and deformed right auricular pavilion (pabellon auricular). Because it is a little known clinical entity, this case of a patient having an incomplete Moebius syndrome of vascular and multifactorial cause was presented. 

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Published

2018-12-17

How to Cite

1.
Hernández Suárez D, Blanco Pereira ME, Luna Ceballos EJ, Martínez Leyva G, Hernández Suárez D, Peréz García A. Incomplete Moebius syndrome. Clinical case presentation. Rev Méd Electrón [Internet]. 2018 Dec. 17 [cited 2025 May 10];40(6):2156-68. Available from: https://revmedicaelectronica.sld.cu/index.php/rme/article/view/2375

Issue

Section

Presentation of cases