2022
DOI: 10.1002/ccr3.6715
|View full text |Cite
|
Sign up to set email alerts
|

Moebius syndrome—Case report

Abstract: Moebius Syndrome is a rare multifactorial condition defined by congenital complete or partial VII and VIth cranial nerves palsy and other physical abnormalities. We present the case of a 3 months old infant with Moebius sequence and breathing and eating difficulties, managed by tracheostomy and laryngoplasty.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
1
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 7 publications
0
1
0
Order By: Relevance
“…In the neonatal period, the main focus of Moebius syndrome treatment is to restore normal breathing and feeding function [ 2 ]. Patients with difficulty swallowing or with tongue movements may require feeding tubes in infancy.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In the neonatal period, the main focus of Moebius syndrome treatment is to restore normal breathing and feeding function [ 2 ]. Patients with difficulty swallowing or with tongue movements may require feeding tubes in infancy.…”
Section: Discussionmentioning
confidence: 99%
“…Prevalence is estimated to be 1/250,000 live births [ 1 ]. Involvement of other cranial nerves (III, IV, and IX-XII) may also occur leading to a variety of craniofacial, odontological, orthopedic, and ophthalmological presentations [ 2 ].…”
Section: Introductionmentioning
confidence: 99%
“…Classic MS is characterized by bilateral or unilateral paralysis of cranial nerves VI and VII; however, it can also be associated with other anomalies or syndromes, such as Kallman, Hanhart, or Poland syndrome. In some cases, patients may have a more extensive involvement affection the cranial nerves: Oculomotor (III), pathetic (IV), trigeminal (V), glossopharyngeal (IX), vagus (X), and hypoglossal (XII) [ 7 ]. The most frequent clinical manifestations of the oral and maxillofacial region included inexpressive facies (lack of smile and facial expression), low implantation of the pinna, and deformity of the ears with hearing loss, micrognathia, microstomia, cleft palate, bifid uvula, occlusal problems [ 8 ].…”
Section: Introductionmentioning
confidence: 99%