{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,27]],"date-time":"2026-06-27T06:57:34Z","timestamp":1782543454309,"version":"3.54.5"},"reference-count":8,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2024,12,19]],"date-time":"2024-12-19T00:00:00Z","timestamp":1734566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"},{"start":{"date-parts":[[2024,12,19]],"date-time":"2024-12-19T00:00:00Z","timestamp":1734566400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Hum Genet"],"published-print":{"date-parts":[[2025,3]]},"abstract":"<jats:title>Abstract<\/jats:title>\n          <jats:p>Sex chromosome aneuploidies (SCA) such as Turner, Klinefelter, Jacobs, and Trisomy X syndromes are prevalent genetic disorders with well-established phenotypes. Challenges persist, however, in determining the need for further genetic evaluation in cases of affected individuals exhibiting atypical symptoms. The present study retrospectively examined 54 pediatric patients with an SCA diagnosis at a single institution between January 2015 and December 2023. Twelve patients (22.2%) exhibited a discordant phenotype, of which five were confirmed to have a distinct monogenic disorder, a diagnostic rate of 41.7%. The monogenic conditions identified included DNAH5-related primary ciliary dyskinesia, Burn-McKeown syndrome, Tatton-Brown-Rahman syndrome, SETD1B-related neurodevelopmental disorder, and SET-related disorder. The median age at SCA diagnosis was 3.5 months versus 7.0 years for the second genetic condition, indicating significant diagnostic delays. Our findings highlight the importance of comprehensive genetic evaluation in pediatric patients with SCA who exhibit atypical phenotypes.<\/jats:p>","DOI":"10.1038\/s10038-024-01312-y","type":"journal-article","created":{"date-parts":[[2024,12,19]],"date-time":"2024-12-19T00:06:39Z","timestamp":1734566799000},"page":"177-179","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Ultra-rare monogenic disorders frequently detected among sex chromosome aneuploidy patients with atypical findings"],"prefix":"10.1038","volume":"70","author":[{"given":"Kiana","family":"Magee","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"William","family":"McGonigle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rena","family":"Pressman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Willa","family":"Thorson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Deborah","family":"Barbouth","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9199-9096","authenticated-orcid":false,"given":"Nicholas A.","family":"Borja","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,12,19]]},"reference":[{"key":"1312_CR1","doi-asserted-by":"publisher","first-page":"306","DOI":"10.1016\/S1474-4422(13)70302-8","volume":"13","author":"DS Hong","year":"2014","unstructured":"Hong DS, Reiss AL. 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J Pediatr Endocrinol Metab. 2008;21:621\u20132.","journal-title":"J Pediatr Endocrinol Metab"},{"key":"1312_CR6","first-page":"19","volume":"13","author":"JR Corona-Rivera","year":"2002","unstructured":"Corona-Rivera JR, Corona-Rivera E, Bobadilla-Morales L, Garcia-Cobia TA, Corona-Rivera A. Cleft lip and\/or palate in two cases of 46,X,i(Xq) Turner syndrome. Genet Couns. 2002;13:19\u201322.","journal-title":"Genet Couns"},{"key":"1312_CR7","doi-asserted-by":"publisher","first-page":"32","DOI":"10.1016\/j.seizure.2022.09.010","volume":"102","author":"GB Dell\u2019Isola","year":"2022","unstructured":"Dell\u2019Isola GB, Mencaroni E, Prontera P, Cara GD, Ferraro L, Bonanni P, et al. Clinical and electroencephalographic features of epilepsy in patients with triple X syndrome: a case series. 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