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home > support groups > conditions and diseases > facial differences > treacher collins syndrome
Treacher Collins Syndrome Support GroupsInformation / Diagnosis / Treatment / Prevention
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- External links (marked with an arrow
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- This site is a web directory and does not offer medical advice.
- We cannot take responsibility for information found on listed sites.
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Health News:
MEDLINE/PubMed Database of Research Articles:
Web Directory:
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Gloria Tabb, Living with Treachers Collins Syndrome Description: Gloria Tabb's story, living with treachers collins. (Gloriatabb.com) |
Microtia - Congenital Ear Institute Description: Information on microtia for families and health care providers. Spanish version as alternative. (microtia.net) |
The Treacher Collins Family Support Group Description: Information regarding the syndrome, genetics, hearing aids, links and support groups. (treachercollins.net) |
Treacher Collins Connection Description: Building a community of people with Treacher Collins syndrome and their families in an environment that transforms people through face to face sharing of experiences, heartaches, and love. (tcconnection.org) |
Treacher Collins Foundation Description: An organization of families, individuals, and professionals who are developing and sharing knowledge about Treacher Collins syndrome. (treachercollinsfnd.org) |
Treacher Collins Syndrome - A Personal View Description: Information, personal insight, discussion forum and the exclusive "TCS Around the World" feature. (treachercollins.co.uk) |
Notes: Healthcyclopedia presents health information in the form of websites and articles that encompass conventional medicine and alternative treatments. Under no circumstances can it recommend or endorse a specific therapy or treatment.
Symptoms should always be presented to a doctor for tests, diagnosis and possible treatment.
Prescription medication should always be taken under a doctor's care.
Also pictures on health websites may occasionally be too graphic for younger viewers.
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