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Waardenburg syndrome with dry eyes: A rare association
Waardenburg syndrome (WS) is a rare congenital disorder primarily characterized by characteristic facial abnormalities as dystopia canthorum and synophrys; depigmentation of the hair, skin (premature graying of hair), and/or the iris of both eyes; and/or congenital deafness. Here, we report a rare c...
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| Publicado no: | Taiwan J Ophthalmol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6759548/ https://ncbi.nlm.nih.gov/pubmed/31572658 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/tjo.tjo_103_18 |
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