Co-occurrence of Neurofibromatosis Type 1 with Tectal Glioma and Acquired Bilateral Nevus of Ota-like Macules
Neurofibromatosis type 1 (NF1) is a common genetic condition characterized by a variety of clinical characteristics such as skeletal deformities, neurofibromas, Lisch nodules, and café-au-lait macules. This case report details a 22-year-old female patient’s unusual co-occurrence of NF1, tectal gliom...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-07-01
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| Series: | Clinical Dermatology Review |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/cdr.cdr_158_24 |
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