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Primary studies presenting results on at least six individuals aged 0\u201018\u00a0years with Marfan syndrome, diagnosed according to the Ghent nosology, were selected.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>From 2341 de\u2010duplicated records, 92 papers were included, mapped and described. Their topics were diagnostics (12%), cardiovascular matters (50%), skeletal matters (22%), ocular matters (9%), other medical aspects (5%) and psychosocial perspectives (2%). Most studies were from Europe and North America and published between 1999 and 2019 in subject\u2010specific or paediatric journals, while a few were published in genetics journals. All studies had quantitative designs, and very few were multicentre studies. Each study had six to 608 subjects for a total of approximately 5809.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>A wide range of research topics on adolescent and paediatric Marfan syndrome was found, but qualitative studies and a focus on psychosocial matters were lacking. Future investigations addressing noncardiovascular consequences and patient experiences are needed, as well as studies reaffirming or replicating existing intervention study results.<\/jats:p><\/jats:sec>","DOI":"10.1111\/apa.15186","type":"journal-article","created":{"date-parts":[[2020,1,24]],"date-time":"2020-01-24T13:59:55Z","timestamp":1579874395000},"page":"1758-1771","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["A scoping review presenting a wide variety of research on paediatric and adolescent patients with Marfan syndrome"],"prefix":"10.1111","volume":"109","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1534-5178","authenticated-orcid":false,"given":"Ingeborg Beate","family":"Lidal","sequence":"first","affiliation":[{"name":"TRS Resource Centre for Rare Disorders Sunnaas Rehabilitation Hospital Oslo Norway"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Trine","family":"Bathen","sequence":"additional","affiliation":[{"name":"TRS Resource Centre for Rare Disorders Sunnaas Rehabilitation Hospital Oslo Norway"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Heidi","family":"Johansen","sequence":"additional","affiliation":[{"name":"TRS Resource Centre for Rare Disorders Sunnaas Rehabilitation Hospital Oslo Norway"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gry","family":"Velvin","sequence":"additional","affiliation":[{"name":"TRS Resource Centre for Rare Disorders Sunnaas Rehabilitation Hospital Oslo Norway"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2020,2,17]]},"reference":[{"key":"e_1_2_10_2_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2008-0703"},{"key":"e_1_2_10_3_1","doi-asserted-by":"publisher","DOI":"10.1038\/ejhg.2008.207"},{"issue":"5","key":"e_1_2_10_4_1","first-page":"262","article-title":"Difficulties in diagnosing Marfan's syndrome in childhood and adolescence. 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