{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T23:39:57Z","timestamp":1792798797751,"version":"4.5.0"},"reference-count":51,"publisher":"BMJ","issue":"4","license":[{"start":{"date-parts":[[2023,11,18]],"date-time":"2023-11-18T00:00:00Z","timestamp":1700265600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000833","name":"Rosetrees Trust","doi-asserted-by":"publisher","award":["PGS19-2\/10111"],"award-info":[{"award-number":["PGS19-2\/10111"]}],"id":[{"id":"10.13039\/501100000833","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100010269","name":"Wellcome Trust","doi-asserted-by":"publisher","award":["WT093113MA"],"award-info":[{"award-number":["WT093113MA"]}],"id":[{"id":"10.13039\/100010269","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["J Med Genet"],"accepted":{"date-parts":[[2023,10,17]]},"published-print":{"date-parts":[[2024,4]]},"abstract":"<jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>Collagen XVII is most typically associated with human disease when biallelic <jats:italic>COL17A1<\/jats:italic> variants (&gt;230) cause junctional epidermolysis bullosa (JEB), a rare, genetically heterogeneous, mucocutaneous blistering disease with amelogenesis imperfecta (AI), a developmental enamel defect. Despite recognition that heterozygous carriers in JEB families can have AI, and that heterozygous <jats:italic>COL17A1<\/jats:italic> variants also cause dominant corneal epithelial recurrent erosion dystrophy (ERED), the importance of heterozygous <jats:italic>COL17A1<\/jats:italic> variants causing dominant non-syndromic AI is not widely recognised.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Probands from an AI cohort were screened by single molecule molecular inversion probes or targeted hybridisation capture (both a custom panel and whole exome sequencing) for <jats:italic>COL17A1<\/jats:italic> variants. Patient phenotypes were assessed by clinical examination and analyses of affected teeth.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Nineteen unrelated probands with isolated AI (no co-segregating features) had 17 heterozygous, potentially pathogenic <jats:italic>COL17A1<\/jats:italic> variants, including missense, premature termination codons, frameshift and splice site variants in both the endo-domains and the ecto-domains of the protein. The AI phenotype was consistent with enamel of near normal thickness and variable focal hypoplasia with surface irregularities including pitting.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>These results indicate that <jats:italic>COL17A1<\/jats:italic> variants are a frequent cause of dominantly inherited non-syndromic AI. Comparison of variants implicated in AI and JEB identifies similarities in type and distribution, with five identified in both conditions, one of which may also cause ERED. Increased availability of genetic testing means that more individuals will receive reports of heterozygous <jats:italic>COL17A1<\/jats:italic> variants. We propose that patients with isolated AI or ERED, due to <jats:italic>COL17A1<\/jats:italic> variants, should be considered as potential carriers for JEB and counselled accordingly, reflecting the importance of multidisciplinary care.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1136\/jmg-2023-109510","type":"journal-article","created":{"date-parts":[[2023,11,18]],"date-time":"2023-11-18T13:20:48Z","timestamp":1700313648000},"page":"347-355","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":10,"title":["Heterozygous <i>COL17A1<\/i> variants are a frequent cause of amelogenesis imperfecta"],"prefix":"10.1136","volume":"61","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4486-1625","authenticated-orcid":false,"given":"Ummey","family":"Hany","sequence":"first","affiliation":[{"name":"Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2371-1844","authenticated-orcid":false,"given":"Christopher M","family":"Watson","sequence":"additional","affiliation":[{"name":"Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK"},{"name":"North East and Yorkshire Genomic Laboratory Hub, Central Lab, St. James's University Hospital, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lu","family":"Liu","sequence":"additional","affiliation":[{"name":"Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK"},{"name":"School of Dentistry, Clarendon Way, University of Leeds, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claire E L","family":"Smith","sequence":"additional","affiliation":[{"name":"Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Asmaa","family":"Harfoush","sequence":"additional","affiliation":[{"name":"School of Dentistry, Clarendon Way, University of Leeds, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2048-5693","authenticated-orcid":false,"given":"James A","family":"Poulter","sequence":"additional","affiliation":[{"name":"Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Georgios","family":"Nikolopoulos","sequence":"additional","affiliation":[{"name":"Institute for Fundamental Biomedical Research, B.S.R.C. 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