1. 
   Waardenburg syndrome
   Waardenburg syndrome: A genetic disorder that causes deafness, white forelock (a frontal white blaze of hair), a difference of color between the iris of one eye and the other (heterochromia iridis), white eye lashes, and wide-set inner corners of the eyes. The deafness is typically congenital (prese...
   Found op http://www.medterms.com/script/main/art.html?articlekey=13431
   
   
2. 
   Waardenburg syndrome
   <syndrome> Rare, autosomal dominant disease with variable penetrance and several known clinical types. ... Clinical features include depigmentation of the skin and hair with a white forelock, congenital cochlear deafness, heterochromia iridis or hypochromia iridis, medial eyebrow hyperplasia, ...
   Found op http://www.mondofacto.com/facts/dictionary?Waardenburg+syndrome
   
   
3. 
   Waardenburg syndrome
   (vahr´den-boorg) any of several hereditary conditions characterized principally by a combination of ear defects and abnormalities of pigment. There may be pigmentary irregularities of the iris and retinal fundus; a patch of white hair or white eyelashes; leukoderma; and cochlear hearing loss. The u...
   Found op http://www.encyclo.co.uk/local/21001
   
   
4. 
   Waardenburg syndrome
   Waardenburg syndrome (also Waardenburg­ Shah Syndrome, Waardenburg-Klein syndrome, Mende`s syndrome II, Van der Hoeve-Halbertsma-Waardenburg syndrome, Ptosis-Epicanthus syndrome, Van der Hoeve-Halbertsma-Gualdi syndrome, Waardenburg type Pierpont,[5] Van der Hoeve-Waardenburg-Klein syndrome, Waar...
   Found op http://en.wikipedia.org/wiki/Waardenburg_syndrome
   
   
5. 
   Waardenburg syndrome
   Waardenburg syndrome (WS) is an inherited disorder often characterized by varying degrees of hearing loss and changes in skin and hair pigmentation. The syndrome got its name from a Dutch eye doctor named Petrus Johannes Waardenburg who first noticed that people with differently colored eyes often h...
   Found op http://www.daviddarling.info/encyclopedia/W/Waardenburg_syndrome.html
   
   
6. 
   Waardenburg Syndrome
   An inherited birth defect in which a baby will suffer from hearing loss and problems with the pigment in the skin and hair. Common symptoms of the disorder include eyes that are different colors or abnormally pale blue eyes, grey hair at any early age, a white patch of hair, white patches in the hai...
   Found op http://www.pregnology.com/AZ/W/1
   
   
7. 
   Waardenburg syndrome
   Type: Term Pronunciation: văr-den-berg Definitions: 1. disorder characterized by lateral displacement of inner canthi (dystopia canthorum), broad nasal root, heterochromia iridis, sensory hearing impairment, white forelock, and synophrys; autosomal dominant inheritance with type 1 distinguished...
   Found op http://www.medilexicon.com/medicaldictionary.php?t=88372
   
   
8. 
   Waardenburg syndrome
   Type: Term Pronunciation: văr-den-berg Definitions: 1. disorder characterized by lateral displacement of inner canthi (dystopia canthorum), broad nasal root, heterochromia iridis, sensory hearing impairment, white forelock, and synophrys; autosomal dominant inheritance with type 1 distinguished...
   Found op http://www.medilexicon.com/medicaldictionary.php?t=89015
   
   
9. 
   Waardenburg-Shah syndrome
   (vahr´den-boorg shah´) Waardenburg syndrome type 4.
   Found op http://www.encyclo.co.uk/local/21001
   
   
10. 
    Waardenburg-Shah syndrome
    Postcard: Bird`s Eye View, Torrington, Connecticut Postmark: 1906 Description: "Old Postcard showing a "Bird`s Eye View" of Torrington, Connecticut. Postmarked 07/26/1906 on an UNdivided back. Published by THe American News Company - New York." Source: eBay auction Web page http://cgi.ebay.com/Old-...
    Found op http://en.wikipedia.org/wiki/Waardenburg-Shah_syndrome
    
    
11. 
    Waardenburg's syndrome
    Autosomal dominant disorder with deafness and pigmentary disturbances probably as a result of defects in function of neural crest. Various forms of the syndrome are recognized. Waardenburg Syndrome 1 (WS1) and WS3 (also known as Klein-Waardenburg syndrome) are caused by mutation in Pax3 - an homolog...
    Found op http://www.encyclo.co.uk/visitor-contributions.php
    
    

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