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A patient with loss of vision in the right eye and neurofibromatosis type 1
Abstract: Neurofibromatosis type 1 is a common autosomal dominant condition that affects about 1 in 5000 people. We describe a 75-year-old man who, in addition to many classic developmental changes of the disease in his skin, eyes and nervous system, had blindness in his right eye as a complication.
Sparad:
| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Canadian Medical Association
2009
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2621301/ https://ncbi.nlm.nih.gov/pubmed/19153396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1503/cmaj.080706 |
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