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Familial bilateral combined hamartoma of retina and retinal pigment epithelium associated with neurofibromatosis 1
We report a family of three siblings followed between 2005 and 2011 with bilateral combined hamartoma of the retina and retinal pigment epithelium, with the age of diagnosis ranging from 7 to 13 years. The main reason for consultation was reduction of vision and squint. The diagnosis was determined...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3729831/ https://ncbi.nlm.nih.gov/pubmed/23960997 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sjopt.2012.03.005 |
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