Frequently Asked Questions
This page is mostly for those doing research projects or something of the like about Treacher Collins syndrome. I have many people emailing me questions for their research project, and often the questions are very similar. So to save time for everyone, I posted the answers to some of the more frequently asked questions. The answers to more questions will be posted at a later date.
Q: Can I use information or pictures
from your webpage for my report/project/research paper/etc.?
Q: Can you send me more info on TCS?
A: No. All the info I have is on my webpage, or can be found
on the other websites to which I have links to on my links page.
Q: What is TCS?
A: Treacher Collins Syndrome is a genetic, craniofacial birth defect.
About one in ten thousand babies are born with it. It is characterized by
depressed cheekbones, malformed or absent ears, a receding chin, and down-slanted
eyes.
Q: What is the cause of TCS?
Q: Does TCS get worse with time?
A: TCS does *NOT* progress or worsen
with time. For example, a person who is born with a mild case of TCS will
*NOT* develop a more severe case of TCS as time goes on.
Q: What is the lifespan of someone with
TCS?
A: TCS does not inherently shorten
someone's lifespan. Some babies are born with very severe cases of TCS and
can die in infancy due to airway or other complications. Otherwise, people
with Treacher Collins syndrome will live as long as the average person.
Q: Do you have a hearing loss?
A: Yes, I have a severe bilateral conductive hearing loss
(about a 60 decibel loss in both ears).
Q: Do you wear a hearing aid?
A: Yes, I wear an bone conduction hearing aid. (See www.treachercollins.org/hrgaid.html)
I have almost normal hearing with my hearing aid.
Copyright © 2004 Amie Osborn. All rights Reserved
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