Waardenburg Syndrome
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Waardenburg Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Waardenburg syndrome is a rare disease characterized by deafness in association with pigmentary anomalies and defects of neural crest-derived tissues. Hammerschlag, in 1907, and Urbantschitsch, in 1910, both mentioned heterochromia iridium and partial albinism as occurring ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:11 pm By:
Julie Bohlen Health Executive and Active Health Library
Waardenburg syndrome is a rare disease characterized by deafness and skin problems. Learn about the cause. http://bit.ly/anSnvq
Waardenburg syndrome...anyone else have this? - TuDiabetes
tudiabetes.com — “if you have, know of, or know someone with this genetic disorder please contact me asap. ty.” View full resource at tudiabetes.com
Most Recently Shared on October 30, 2009 at 9:03 am By:
Type 1 diabetes: Waardenburg syndrome...anyone else have this?: if you have, know of, or know.. http://bit.ly/esB6j
Congenital Patterned Leukodermas: eMedicine Dermatology
emedicine.medscape.com — “Overview: The following congenital hypopigmentary diseases result from a failure of pigment cells (melanocytes) in the skin, eyes, and/or ears to become completely or partially established in their target sites during embryogenesis:Waardenburg syndrome (types I, II, and ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 18, 2010 at 7:36 pm By:
Julie Bohlen Health Executive and Active Health Library
Congenital patterned leukodermas are disorders in which pigments did not properly form in the womb. Learn more. http://bit.ly/9hB2D1
Mutations in the SPARC-Related Modular Calcium-Bin... [Am J Hum Genet. 2011] - PubMed result
ncbi.nlm.nih.gov — “PubMed is a service of the U.S. National Library of Medicine that includes over 19 million citations from MEDLINE and other life science journals for biomedical articles back to the 1950s. PubMed includes links to full text articles and other related resources.” View full resource at ncbi.nlm.nih.gov
Most Recently Shared on January 10, 2011 at 9:58 pm By:
Jon D. Moulton PhD, Active Health Library, Doctor, and Science Enthusiast
Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome. http://bit.ly/gwaMzo
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Julie Bohlen
Health content professional with MBA in heathcare management. Sharing quality health resources and news. On executive team at OrganizedWisdom.
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a diabetes community
A nonprofit social network with nearly 20K members touched by diabetes run by @DiabetesHF. Some tweets: FC (Fabiana Couto), MH (Manny Hernandez).
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Julie Bohlen
Health content professional with MBA in heathcare management. Sharing quality health resources and news. On executive team at OrganizedWisdom.
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