{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,15]],"date-time":"2025-12-15T19:46:05Z","timestamp":1765827965141,"version":"build-2065373602"},"reference-count":18,"publisher":"BMJ","issue":"10","funder":[{"name":"A Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science","award":["No. 19K09473","No. 19K09499"],"award-info":[{"award-number":["No. 19K09473","No. 19K09499"]}]},{"name":"A research grant from Takeda Science Foundation"},{"name":"A research grant from Japan Intractable Diseases (Nanbyo) Research Foundation"},{"name":"A Grant-in-Aid for Scientific Research (B) from the Japan Society for the Promotion of Science","award":["No. 17H04301"],"award-info":[{"award-number":["No. 17H04301"]}]},{"name":"A MEXT KAKENHI","award":["No. 221S0002"],"award-info":[{"award-number":["No. 221S0002"]}]},{"name":"A Grant-in-Aid for Research Activity Start-up from the Japan Society for the Promotion of Science","award":["No. 19K24023"],"award-info":[{"award-number":["No. 19K24023"]}]}],"content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["J Med Genet"],"accepted":{"date-parts":[[2020,8,4]]},"published-print":{"date-parts":[[2021,10]]},"abstract":"<jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>Although 60% of patients with de novo neurofibromatosis type 2 (NF2) are presumed to have mosaic NF2, the actual diagnostic rate of this condition remains low at around 20% because of the existing difficulties in detecting <jats:italic>NF2<\/jats:italic> variants with low variant allele frequency (VAF). Here, we examined the correlation between the genotype and phenotype of mosaic NF2 after improving the diagnostic rate of mosaic NF2.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>We performed targeted deep sequencing of 36 genes including <jats:italic>NF2<\/jats:italic> using DNA samples from multiple tissues (blood, buccal mucosa, hair follicle and tumour) of 53 patients with de novo NF2 and elucidated their genotype\u2013phenotype correlation.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Twenty-four patients (45.2%) had the <jats:italic>NF2<\/jats:italic> germline variant, and 20 patients with NF2 (37.7%) had mosaic NF2. The mosaic NF2 phenotype was significantly different from that in patients with <jats:italic>NF2<\/jats:italic> germline variant in terms of distribution of NF2-related disease, tumour growth rate and hearing outcome. The behaviour of schwannoma correlated to the extent of VAF with <jats:italic>NF2<\/jats:italic> variant in normal tissues unlike meningioma.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>We have improved the diagnostic rate of mosaic NF2 compared with that of previous studies by targeted deep sequencing of DNA from multiple tissues. Many atypical patients with NF2 diagnosed with \u2018unilateral vestibular schwannoma\u2019 or \u2018multiple meningiomas\u2019 presumably have mosaic NF2. Finally, we suggest that the highly diverse phenotype of NF2 could result not only from the type and location of <jats:italic>NF2<\/jats:italic> variant but also the extent of VAF in the <jats:italic>NF2<\/jats:italic> variant within normal tissue DNA.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1136\/jmedgenet-2020-106973","type":"journal-article","created":{"date-parts":[[2020,10,16]],"date-time":"2020-10-16T17:21:35Z","timestamp":1602868895000},"page":"701-711","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":20,"title":["Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2"],"prefix":"10.1136","volume":"58","author":[{"given":"Yu","family":"Teranishi","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, The University of Tokyo, Bunkyo-ku, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6369-3391","authenticated-orcid":false,"given":"Satoru","family":"Miyawaki","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, The University of Tokyo, Bunkyo-ku, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroki","family":"Hongo","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, The University of Tokyo, Bunkyo-ku, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shogo","family":"Dofuku","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, The University of Tokyo, Bunkyo-ku, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Atsushi","family":"Okano","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, The University of Tokyo, Bunkyo-ku, Tokyo, 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