Bone absorption and deformity in mandible as initial symptom and manifestation of neurofibromatosis type 1: A case report and literature review

Neurofibromatosis type 1 (NF-1) is an autosomal dominant inherited genodermatosis disease and tumor susceptibility syndrome with a prevalence of 1/6000–1/3000 reported in most epidemiological studies and 1/3333–1/2558 in live births. NF1 is caused by pathogenic variants in the NF1 gene on autosome 1...

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Bibliographic Details
Main Authors: Lini Deng, Yi Wang, Xianwang Xiang, Chuanjun Chen
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:Oral Oncology Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S277290602300122X
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