Find Expert Doctors on Waardenburg syndrome type 2200 top medical experts on Waardenburg syndrome type 2 across 15 countries and 4 U.S. states, including 21 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Waardenburg syndrome type 2: An autosomal dominant subtype of Waardenburg syndrome (WS) characterized by varying degrees of deafness and pigmentation anomalies of eyes, hair and skin, but without dystopia canthorum.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- American Society for Deaf Children (ASDC)
PO Box 23
Woodbine, MD 21797
Toll-free: 1-800-942-2732
E-mail: info@deafchildren.org
Website: http://deafchildren.org/
- National Association of the Deaf
8630 Fenton Street Suite 820
Silver Spring, MD 20910
Telephone: +1-301-587-1788
TTY: +1-301-587-1789
Fax: +1-301-587-1791
E-mail: NADinfo@nad.org
Website: https://www.nad.org/
- The National Organization of Albinism and Hypopigmentation (NOAH)
PO Box 959
East Hampstead, NH 03826-0959
Toll-free: 800-473-2310;
Telephone: 603-887-2310
E-mail: noah@albinism.org
Website: http://www.albinism.org
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Organizations Providing General Support
- The Vision of Children Foundation (VOC)
12555 High Bluff Drive, Suite 330
San Diego, CA 92130
Telephone: +1-858-314-7916
E-mail: info@visionofchildren.org
Website: https://www.visionofchildren.org/
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