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Waardenburg syndrome: A rare genetic disorder, a report of two cases
Waardenburg syndrome (WS) is a rare genetic disorder. Patients have heterochromia or eyes with iris of different color, increased inter-canthal distance, distopia canthorum, pigmentation anomalies, and varying degree of deafness. It usually follows autosomal dominant pattern. In this report, two cas...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3491306/ https://ncbi.nlm.nih.gov/pubmed/23162308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.100804 |
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