Treacher Collins syndrome (TCS) is a rare autosomal dominant congenital
disorder characterized by craniofacial deformities, such as absent cheekbones.
2 days ago ... Treacher Collins syndrome is a condition that affects the development of bones
and other tissues of the face. The signs and symptoms of this ...
Dec 9, 2014 ... Read about Treacher Collins syndrome, a rare genetic condition that affects the
development of the bones and tissues of the face. Read about ...
Treacher Collins syndrome: Treacher Collins is a condition in which the cheek-
bones and jawbones are underdeveloped. Children with this condition have very
Feb 9, 2016 ... Mandibulofacial dysostosis, also known as Treacher Collins syndrome (TCS;
entry 154500 in the Online Mendelian Inheritance in Man [OMIM] ...
Signs and symptoms of Treacher Collins syndrome can include differences in the
cheekbones, brow bones, eyelids, ears, mouth, jaws and teeth.
Treacher Collins syndrome is a rare condition that affects the face. It is caused by
a genetic mutation that happens before birth.
A number sign (#) is used with this entry because Treacher Collins syndrome-1 is
caused by heterozygous mutation in the 'treacle' gene (TCOF1; 606847) on ...
A number sign (#) is used with this entry because Treacher Collins syndrome-3 (
TCS3) is caused by compound heterozygous mutation in the POLR1C gene ...
A number sign (#) is used with this entry because Treacher Collins syndrome-2
can be caused by heterozygous mutation in the POLR1D gene (613715) on ...