Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. The degree to which a person is affected can vary from mild to severe. Complications may include breathing problems, problems seeing, cleft palate, and hearing loss.
Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. The degree to which a person is affected can vary from mild to severe. Complications may include breathing problems, problems seeing, cleft palate, and hearing loss.
If your child has been diagnosed with Treacher Collins Syndrome, we understand how difficult it is not only to sort through the emotional aspects of this, but also to find the right information and especially the right help. To all these parents, we want to say take heart. There is hope, and you’re in the right place.
At Little Baby Face Foundation, Treacher Collins Syndrome is something we see and treat frequently. We help parents understand their options and make educated decisions on their child’s medical path, and we help the children feel as comfortable, safe, and loved as possible. Children stay with the foundation until they are 21 years of age, giving us a chance to forge personal relationships with them, but more importantly, to be able to address their TCS as they grow and develop.
We pair our close care for families with a wealth of expertise. Little Baby Face Foundation has leading experts in treating children with Treacher Collins Syndrome. Dr. Thomas Romo, for example, is a world leader in auricular reconstruction (reconstruction of the ear or ears). Dr. Darius Kohan is a leading Otolaryngologist (an ear, nose, and throat doctor). Together, Dr. Romo and Dr. Kohan are able to build a child’s ears and help him or her to hear.
At Little Baby Face Foundation, Treacher Collins Syndrome is something we see and treat frequently. We help parents understand their options and make educated decisions on their child’s medical path, and we help the children feel as comfortable, safe, and loved as possible. Children stay with the foundation until they are 21 years of age, giving us a chance to forge personal relationships with them, but more importantly, to be able to address their TCS as they grow and develop.
If your child has been diagnosed with Treacher Collins Syndrome, we understand how difficult it is not only to sort through the emotional aspects of this, but also to find the right information and especially the right help. To all these parents, we want to say take heart. There is hope, and you’re in the right place.
At Little Baby Face Foundation, Treacher Collins Syndrome is something we see and treat frequently. We help parents understand their options and make educated decisions on their child’s medical path, and we help the children feel as comfortable, safe, and loved as possible. Children stay with the foundation until they are 21 years of age, giving us a chance to forge personal relationships with them, but more importantly, to be able to address their TCS as they grow and develop.
We pair our close care for families with a wealth of expertise. Little Baby Face Foundation has leading experts in treating children with Treacher Collins Syndrome. Dr. Thomas Romo, for example, is a world leader in auricular reconstruction (reconstruction of the ear or ears). Dr. Darius Kohan is a leading Otolaryngologist (an ear, nose, and throat doctor). Together, Dr. Romo and Dr. Kohan are able to build a child’s ears and help him or her to hear.
At Little Baby Face Foundation, Treacher Collins Syndrome is something we see and treat frequently. We help parents understand their options and make educated decisions on their child’s medical path, and we help the children feel as comfortable, safe, and loved as possible. Children stay with the foundation until they are 21 years of age, giving us a chance to forge personal relationships with them, but more importantly, to be able to address their TCS as they grow and develop.
Hope and Inspiration: Please click on the media logos below to read the two articles on Jared Galicia's Journey with Treacher Collins Syndrome.
Hope and Inspiration: Please click on the media logos below to read the two articles on Jared Galicia's Journey with Treacher Collins Syndrome.
If you’re new to this and wondering where to start, please complete the form below so we can get you on the right path. You’re not alone in this, and help is here for you whenever you’re ready.
If you’re new to this and wondering where to start, please complete the form below so we can get you on the right path. You’re not alone in this, and help is here for you whenever you’re ready.