Extensive Peculiar Cutaneous Form of Neurofibromatosis Type I as a New Mutation - a Case Report
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease manifests a variety of characteristic features that include: hyperpigmentary abnormalities of the skin (café-au-lait macules, freckles in the axillae, and iris Lisch nodules) and growth of benign peri...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Sciendo
2016-03-01
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| Series: | Serbian Journal of Dermatology and Venereology |
| Subjects: | |
| Online Access: | https://doi.org/10.1515/sjdv-2016-0002 |