Diagnosis and treatment of Treacher Collins syndrome: Report of a rare case with literature review

• Main Authors: Ananya Madiyal (Author), Subhas G Babu (Author), Supriya Bhat (Author), Medhini Madi (Author), Jasmine Kamath (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2017-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Treacher Collins syndrome is a rare genetic disorder that affects one in 50,000 live births with no gender predilection. It occurs due to defect in the development of structures derived from the first and second branchial arches, grooves, and pouches. Mutation of the TCOF1, POLR1C, and POLR1D genes...