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Revista Médica Electrónica
versión On-line ISSN 1684-1824
Resumen
HERNANDEZ SUAREZ, Damarys et al. Incomplete Moebius syndrome. Clinical case presentation. Rev.Med.Electrón. [online]. 2018, vol.40, n.6, pp. 2120-2139. ISSN 1684-1824.
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.
Palabras clave : Moebius syndrome; congenital facial paralysis; congenital paralysis of the VI and VII cranial nerves nuclei.