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Semaphorin-plexin signalling controls cellular interactions that are critical during development as well as in adult life stages. Nine plexin genes have been identified in humans, but despite the apparent importance of plexins in development, only biallelic <jats:italic>PLXND1<\/jats:italic> and <jats:italic>PLXNA1<\/jats:italic> variants have so far been associated with Mendelian genetic disease.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Eight individuals from six families presented with a recessively inherited variable clinical condition, with core features of amelogenesis imperfecta (AI) and sensorineural hearing loss (SNHL), with variable intellectual disability. Probands were investigated by exome or genome sequencing. Common variants and those unlikely to affect function were excluded. Variants consistent with autosomal recessive inheritance were prioritised. Variant segregation analysis was performed by Sanger sequencing. RNA expression analysis was conducted in C57Bl6 mice.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Rare biallelic pathogenic variants in plexin B2 (<jats:italic>PLXNB2<\/jats:italic>), a large transmembrane semaphorin receptor protein, were found to segregate with disease in all six families. The variants identified include missense, nonsense, splicing changes and a multiexon deletion. <jats:italic>Plxnb2<\/jats:italic> expression was detected in differentiating ameloblasts.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>We identify rare biallelic pathogenic variants in <jats:italic>PLXNB2<\/jats:italic> as a cause of a new autosomal recessive, phenotypically diverse syndrome with AI and SNHL as core features. Intellectual disability, ocular disease, ear developmental abnormalities and lymphoedema were also present in multiple cases. The variable syndromic human phenotype overlaps with that seen in <jats:italic>Plxnb2<\/jats:italic> knockout mice, and, together with the rarity of human <jats:italic>PLXNB2<\/jats:italic> variants, may explain why pathogenic variants in <jats:italic>PLXNB2<\/jats:italic> have not been reported previously.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1136\/jmg-2023-109728","type":"journal-article","created":{"date-parts":[[2024,3,8]],"date-time":"2024-03-08T13:21:01Z","timestamp":1709904061000},"page":"689-698","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":7,"title":["Biallelic variants in Plexin B2 (<i>PLXNB2<\/i>) cause amelogenesis imperfecta, hearing loss and intellectual disability"],"prefix":"10.1136","volume":"61","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8320-5105","authenticated-orcid":false,"given":"Claire E L","family":"Smith","sequence":"first","affiliation":[{"name":"Institute of Medical Research, 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