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How does the Precision Peptide Genetic Test improve my results
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A diagnosis of Schwannoma is made using the following tools: Complete physical examination with thorough evaluation of the individuals medical history (including family history of neurofibromatosis type 2 or Schwannoma) Neurological exam of the entire body Radiological studies (CT, MRI scan) of the affected region Nerve conduction studies of the affected nerve Other specific tests may be conducted based on the location of the tumor Tissue biopsy: A tissue biopsy is performed and sent to a laboratory for a pathological examination, who examines the biopsy under a microscope
doi: 10.3389/fcimb.2025.1662442 Received 09 July 2025 Accepted 18 August 2025 Published 25 September 2025 Volume 15 - 2025 Edited by Yuanwei Zhang, Nanjing Normal University, China Reviewed by Estela Ruiz-Baca, Jurez University of the State of Durango, Mexico Antonio Vitiello, Ministry of Health, Rome, Italy Hu Pengjie, Chinese Academy of Sciences (CAS), China Updates Copyright 2025 Li, Liu, Jiang, Yang, Ni, Zhang and Tan
