Wildervanck's syndrome with severe inner ear dysplasia and agenesis of the right internal carotid artery

Wildervanck's syndrome with severe inner ear dysplasia and agenesis of the right internal carotid artery

Abstract We describe a case with Wildervanck syndrome (cervico-oculo-acoustic syndrome) comprising Klippel–Feil anomaly, retractio bulbi (Duane syndrome), and congenital sensorineural deafness. An 18-month male baby had a severe inner ear dysplasia, and MRI also showed a complex vascular carotid mal...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of pediatric otorhinolaryngology 2014-04, Vol.78 (4), p.704-706
Hauptverfasser: Hernando, Mónica, Urbasos, María, Amarillo, Viviana Elizabeth, Herrera, María Teresa, García-Peces, Victoria, Plaza, Guillermo
Format: Artikel
Sprache:eng
Schlagworte:
Abnormalities, Multiple - diagnosis
Carotid Artery, Internal - abnormalities
Cervico-oculo-acustic
Ear, Inner - abnormalities
Heart Defects, Congenital - diagnosis
Heart Septal Defects, Atrial - diagnosis
Humans
Infant
Inner ear aplasia
Internal carotid aplasia
Lower Extremity Deformities, Congenital - diagnosis
Magnetic Resonance Imaging - methods
Male
Otolaryngology
Pediatrics
Rare Diseases
Risk Assessment
Tomography, X-Ray Computed - methods
Upper Extremity Deformities, Congenital - diagnosis
Vascular Malformations - diagnosis
Wildervanck
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Abstract We describe a case with Wildervanck syndrome (cervico-oculo-acoustic syndrome) comprising Klippel–Feil anomaly, retractio bulbi (Duane syndrome), and congenital sensorineural deafness. An 18-month male baby had a severe inner ear dysplasia, and MRI also showed a complex vascular carotid malformation associated.
ISSN:0165-5876
1872-8464
DOI:10.1016/j.ijporl.2014.01.036