Year: 2025
Type: preprint
Study design: Case Report
Abstract: IntroductionNeurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders, with an estimated prevalence of 1 in 2,500 to 3,000 individuals worldwide. It results from pathogenic variants in the NF1 gene on chromosome 17,
Authors: Mehdi Abrishami, Hamid Taherinya, Seyed Amir Masoud Mousavi, Amirmansour shirani
Institution: Islamic Azad University, Isfahan
Language: English
Subfield: Periodontics
Field: Dentistry
Domain: Health Sciences
Open Access status: gold
Funder: Islamic Azad University
OpenAlex ID: W4415024888
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