AbstractObjectiveTo describe a case of hearing rehabilitation with bone anchored hearing aid in a patient with Treacher Collins syndrome.Case description3 years old patient, male, with Treacher Collins syndrome and severe complications due to the syndrome, mostly related to the upper airway and hearing. He had bilateral atresia of external auditory canals, and malformation of the pinna. The initial hearing rehabilitation was with bone vibration arch, but there was poor acceptance due the discomfort caused by skull compression. It was prescribed a model of bone-anchored hearing aid, in soft band format. The results were evaluated through behavioral hearing tests and questionnaires Meaningful Use of Speech Scale (MUSS) and Infant-Toddler Mean...
OBJECTIVE: To study the audiologic outcome of bone-anchored hearing aid (BAHA) application in patien...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Introduction: Treacher Collins Syndrome (TCS) is an inherited and rare, autosomal dominant condition...
AbstractObjectiveTo describe a case of hearing rehabilitation with bone anchored hearing aid in a pa...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
Item does not contain fulltextAbout 50% of patients with the TCS have conductive hearing loss, cause...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background: Management of patients with Treacher Collins syndrome is complicated and involves multip...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Item does not contain fulltextOBJECTIVES: To study the benefit of the application of a bone-anchored...
OBJECTIVES: To study the benefit of the application of a bone-anchored hearing aid in patients with ...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
Objective: Treacher Collins syndrome or mandibulofacial dysostosis is a rare genetic syndrome charac...
Contains fulltext : 70824.pdf (publisher's version ) (Closed access)In 1984 the Bo...
Apresentamos o caso de um menino de 8 anos de idade referenciado ao serviço de otorrinolaringologia ...
OBJECTIVE: To study the audiologic outcome of bone-anchored hearing aid (BAHA) application in patien...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Introduction: Treacher Collins Syndrome (TCS) is an inherited and rare, autosomal dominant condition...
AbstractObjectiveTo describe a case of hearing rehabilitation with bone anchored hearing aid in a pa...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
Item does not contain fulltextAbout 50% of patients with the TCS have conductive hearing loss, cause...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background: Management of patients with Treacher Collins syndrome is complicated and involves multip...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Item does not contain fulltextOBJECTIVES: To study the benefit of the application of a bone-anchored...
OBJECTIVES: To study the benefit of the application of a bone-anchored hearing aid in patients with ...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
Objective: Treacher Collins syndrome or mandibulofacial dysostosis is a rare genetic syndrome charac...
Contains fulltext : 70824.pdf (publisher's version ) (Closed access)In 1984 the Bo...
Apresentamos o caso de um menino de 8 anos de idade referenciado ao serviço de otorrinolaringologia ...
OBJECTIVE: To study the audiologic outcome of bone-anchored hearing aid (BAHA) application in patien...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Introduction: Treacher Collins Syndrome (TCS) is an inherited and rare, autosomal dominant condition...