License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40 % of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies. Mild cases of TCS often pass undiagnosed at birth or early childhood. The disease may be manifested as conductive hearing loss in teenagers and may resemble juvenile otosclerosis. Patients could suffer from slight facial variabilities including retrognathia (as in our case) and others, which point out to a possible middle ear anomaly. Surgical corrections of middle ear anomalies including TCS generally lead to poorer outcome...
Published online 1 September 2004To define the range of phenotypic expression in Treacher Collins sy...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of facial development, which resul...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
Item does not contain fulltextAbout 50% of patients with the TCS have conductive hearing loss, cause...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
Introduction: Treacher Collins Syndrome (TCS) is an inherited and rare, autosomal dominant condition...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second ...
Treacher Collins syndrome (TCS) or Franceschetti syndrome is an autosomal dominant disorder of crani...
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...
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by ...
Treacher Collins syndrome is a rare autosomal dominant condition, predominantly affecting the orofac...
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. M...
Published online 1 September 2004To define the range of phenotypic expression in Treacher Collins sy...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of facial development, which resul...
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals...
Item does not contain fulltextAbout 50% of patients with the TCS have conductive hearing loss, cause...
About 50% of patients with the TCS have conductive hearing loss, caused by characteristic major and/...
Introduction: Treacher Collins Syndrome (TCS) is an inherited and rare, autosomal dominant condition...
Treacher Collins syndrome(TCS) is a rare, incurable condition occurring in approximately 1 of 25,000...
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second ...
Treacher Collins syndrome (TCS) or Franceschetti syndrome is an autosomal dominant disorder of crani...
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...
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by ...
Treacher Collins syndrome is a rare autosomal dominant condition, predominantly affecting the orofac...
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. M...
Published online 1 September 2004To define the range of phenotypic expression in Treacher Collins sy...
Background: Treacher-Collins syndrome is a congenital craniofacial disorder with multiple anomalies....
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of facial development, which resul...