منابع مشابه
Laryngeal cleft type I in neonate: case report.
Laryngeal cleft (LC) is a congenital malformation that leads to the unusual communication between the esophagus and the laryngotracheal complex. It is a rare disease, mostly prevalent among male individuals. The goal of this study was to describe the evaluation and intervention by the speech language pathologist of a female newborn diagnosed with LC type I, admitted on the University Hospital o...
متن کاملType I-II laryngeal cleft: clinical course and outcome.
BACKGROUND Laryngeal cleft (LC) is a rare congenital anomaly manifesting in a variety of symptoms, including swallowing disorders and aspirations, dyspnea, stridor and hoarseness. The mild forms (types I-II) may be underdiagnosed, leading to protracted symptomatology and morbidity. OBJECTIVES To evaluate the diagnostic process, clinical course, management and outcome in children with type I-I...
متن کاملPostoperative observation of children after endoscopic type 1 posterior laryngeal cleft repair.
OBJECTIVES To report the perioperative management and surgical outcomes in a large series of pediatric patients with endoscopically repaired type 1 posterior laryngeal cleft (PLC). STUDY DESIGN Case series with chart review. SETTING Urban, tertiary care, free-standing pediatric hospital. SUBJECTS AND METHODS Patients who underwent endoscopic carbon dioxide laser-assisted repair of type 1 ...
متن کاملType 1 laryngeal cleft: establishing a functional diagnostic and management algorithm.
OBJECTIVES To report our experience with all patients diagnosed with type 1 laryngeal cleft over a period of 3 years in our referral practice and to describe a functional diagnostic and management algorithm for children with this disorder. METHODS A prospective longitudinal study in a tertiary care referral center. Twenty pediatric patients diagnosed with type 1 laryngeal cleft in a 3-year pe...
متن کاملRepair of long type IV posterior laryngeal cleft through a cervical approach using cricotracheal separation.
A female infant with CHARGE syndrome and a long type IV cleft extending to within 5 mm of the carina underwent transcervical repair at 5 weeks of age. The trachea was transected from the cricoid cartilage and was peeled off the esophagus. The front of the esophagus and the back of the trachea were repaired while still ventilating the patient. The trachea was reconnected to the cricoid cartilage...
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ژورنال
عنوان ژورنال: JAMA Otolaryngology–Head & Neck Surgery
سال: 2014
ISSN: 2168-6181
DOI: 10.1001/jamaoto.2013.5739