Waardenburg syndrome type2 in a 10 month old infant; a case report
(Received 17 August, 2009 ; Accepted 9 December, 2009)AbstractBackground and purpose: Waardenburg syndrome (WS) is a rare disease characterized by sensor neural deafness in association with pigmentary anomalies and defects of neural-crest-derived tissues. WS is caused by mutations in the microphthal...
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Mazandaran University of Medical Sciences
2009-01-01
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| Saila: | Journal of Mazandaran University of Medical Sciences |
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| Sarrera elektronikoa: | http://www.mazums.ac.ir/index.php?digital_library&do=downloadPdf&sid=806 |
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