Clinical manifestations and genetic analysis of a family with neurofibromatosis type 2

CONCLUSIONS: Hearing impairment was the most common clinical manifestation in this family. The NF2 gene is a gene of interest that warrants familial genetic screening.PMID:34915804 | DOI:10.1080/00016489.2021.2012594

Source: Acta Oto-Laryngologica - December 17, 2021 Category: ENT & OMF Authors: Victoria Y Wang Te-Yi Liu Te-Yung Fang Ya-Hui Chen Chi-Jung Huang Pa-Chun Wang Source Type: research