Multiple glomus tumor in a patient with neurofibromatosis type 1: a case report and literature review
Neurofibromatosis type I (NF1) is an autosomal dominant disease, with an incidence of 1/2,500-3,000 births and a prevalence of approximately 1/4,000-5,000 individuals. Genetic mutations in the NF1 gene cause it, affecting neural and skin tissues. Glomus tumor is a benign neoplasm originating from th...
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| Main Authors: | , , , |
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| Format: | Book |
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Sociedade Brasileira de Dermatologia (SBD),
2020-12-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |