Item does not contain fulltextAbout 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/or minor ear anomalies. It is also common for these patients to have microtia or severe malformation of the pinna. The results of [figure: see text] reconstructive surgery to improve hearing are usually moderate to poor, because of combinations of anomalies. In general, it is recommended to start hearing rehabilitation at the earliest possible stage. Owing to the above-described anomalies, rehabilitation usually involves fitting a BAHA, whether or not in combination with a pinna epithesis
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. M...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
AbstractObjectiveTo describe a case of hearing rehabilitation with bone anchored hearing aid in a pa...
Contains fulltext : 21858.PDF (publisher's version ) (Open Access
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second ...
Treacher Collins syndrome (TCS) is a rare genetic disorder characterized primarily by abnormalities ...
Objective: Treacher Collins syndrome or mandibulofacial dysostosis is a rare genetic syndrome charac...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Published online 1 September 2004To define the range of phenotypic expression in Treacher Collins sy...
Treacher Collins syndrome (TCS) or Franceschetti syndrome is an autosomal dominant disorder of crani...
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by ...
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. M...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
AbstractObjectiveTo describe a case of hearing rehabilitation with bone anchored hearing aid in a pa...
Contains fulltext : 21858.PDF (publisher's version ) (Open Access
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second ...
Treacher Collins syndrome (TCS) is a rare genetic disorder characterized primarily by abnormalities ...
Objective: Treacher Collins syndrome or mandibulofacial dysostosis is a rare genetic syndrome charac...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Published online 1 September 2004To define the range of phenotypic expression in Treacher Collins sy...
Treacher Collins syndrome (TCS) or Franceschetti syndrome is an autosomal dominant disorder of crani...
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by ...
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. M...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...
Background: Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital ...