Neurofibromatosis Type I (Von Recklinghausen Disease): A Case Report and Review of the Literature
Neurofibromatosis type I is an autosomal dominant genetic disorder with an incidence of about 1 in 3000 births. Apart from the typical skin involvement NF1 may affect multiple organs with ocular, neurological, skeletal and cardiovascular manifestations. We present a case of a 38-year-old man with mu...
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| Main Authors: | , , , , |
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| Format: | article |
| Language: | EN |
| Published: |
Sciendo
2020
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| Subjects: | |
| Online Access: | https://doaj.org/article/ccd91bdf10a24851a3c1063bcabaf0c7 |
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