Congenital facial paralysis - presentation of a clinical case

Authors

  • Asia Asenova UHATNP "St.Naum"; Medical university – Sofia
  • I. Aleksandrova UHATNP "St.Naum"; Medical university – Sofia
  • A. Shokova UHATNP „St. Naum”
  • E. Rodopska UHATNP „St. Naum”
  • N. Topalov UHATNP "St.Naum"; Medical university – Sofia
  • V. Bojinova UHATNP „St. Naum”

Keywords:

Congenital facial paralysis, Moebius syndrome

Abstract

Congenital facial paralysis is presented clinically as decreased or absent movement of the facial muscles, which is found at birth and is due to impaired or completely missing function of the facial nerve. Etiology for disease includes two major groups -intrapartum injury or various developmental disorders.
Facial nerve aplasia is an extremely rare anomaly that usually occurs in association with Moebius syndrome. Moebius syndrome is a rare neurological disorder characterized by weakness or paralysis (palsy) of multiple cranial nerves, most often the 6th (abducens) and 7th (facial) nerves, resulting in limitation of lateral gaze movement and facial diplegia. We present a case of an 8-year-old girl with probable hypoplasia of the nuclei of the facial nerves and the nuclei of nn abducens.
Although aplasia or hypoplasia of the facial nerve is rare, their recognition is clinically important for its prognostic and medicolegal implications.

References

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Published

30.11.2021

How to Cite

Asenova, Asia, et al. “Congenital Facial Paralysis - Presentation of a Clinical Case”. Cephalgia, vol. 23, no. 1, Nov. 2021, pp. 36-40, https://cephalgia.org/index.php/ce/article/view/55.

Issue

Section

CEPHALGIA