Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
Stapes Gusher And Klippel‐Feil Syndrome
View through CrossRef
The stapes gusher which is the most dramatic complication of stapedectomy arises from an abnormal communication between the subarchnoid and perilymphatic spaces. This congenital defect may be associated with other anomalies such as the Klippel‐Feil syndrome. Two cases of stapes gusher in patients with congenital fixation of the footplate are described. One of them was combined with Klippel‐Feil syndrome. The object of this paper is to emphasize the necessity of a complete preoperative examination of all cases of congenital footplate fixation.
Title: Stapes Gusher And Klippel‐Feil Syndrome
Description:
The stapes gusher which is the most dramatic complication of stapedectomy arises from an abnormal communication between the subarchnoid and perilymphatic spaces.
This congenital defect may be associated with other anomalies such as the Klippel‐Feil syndrome.
Two cases of stapes gusher in patients with congenital fixation of the footplate are described.
One of them was combined with Klippel‐Feil syndrome.
The object of this paper is to emphasize the necessity of a complete preoperative examination of all cases of congenital footplate fixation.
Related Results
Preoperative prediction of stapes exposure during otomicrosurgery based on temporal bone computed tomography images：A cohort observational study
Preoperative prediction of stapes exposure during otomicrosurgery based on temporal bone computed tomography images：A cohort observational study
Introduction:
This prospective study aimed to evaluate the
predictive value of high-resolution computed tomography (CT) scan of the
temporal bone in predicting th...
Klippel-Feil syndrome associated with congenital megacolon: a case report
Klippel-Feil syndrome associated with congenital megacolon: a case report
Klippel-Feil syndrome is a congenital abnormality characterized by the fusion of the bones of the cervical spine. Its association with a gastrointestinal abnormality is rare. We re...
Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report
Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report
Klippel-Feil syndrome is defined as congenital fusion of two or more cervical vertebrae. In this article, we report a 55-year-old male patient with one-year history of neck pain, h...
KLIPPEL-FEIL SYNDROME
KLIPPEL-FEIL SYNDROME
Introduction
Klippel-Feil Syndrome is a complex condition, characterized by fusion of cervical vertebrae 2 and 3; however, it has been shown in several studies that fusion of the v...
Tympanoplasty with an Intact Stapes Superstructure in Chronic Otitis Media
Tympanoplasty with an Intact Stapes Superstructure in Chronic Otitis Media
BACKGROUND: The objective of our study was to ascertain the functional results in terms of air bone gap (ABG) closure over 4 frequencies (0.5, 1, 2, 3 kHz) in patients with chronic...
Klippel–Feil Syndrome A Case Report
Klippel–Feil Syndrome A Case Report
Klippel-Feil syndrome is a condition characterized by fusion of the spine owing to the failure of normal segmentation of the cervical structures. In this case report, we aimed to d...
Therapeutic rehabilitation for Klippel-Feil syndrome: a case report
Therapeutic rehabilitation for Klippel-Feil syndrome: a case report
Klippel-Feil syndrome (KFS) is a genetic condition presenting with a triad of symptoms: short neck, limited range of motion in the neck, and a low posterior hair line. Herein, we r...
A modified tracheostomy technique in an adult patient with Klippel-Feil syndrome.
A modified tracheostomy technique in an adult patient with Klippel-Feil syndrome.
Klippel-Feil syndrome is a rare congenital condition characterized by
the fusion of cervical vertebrae, presenting unique challenges for
airway management. We report the case of a ...