Edwards' syndrome.
Crawford D, Dearmun A.
Nurs Child Young People. 2016 Dec 8;28(10):17. doi: 10.7748/ncyp.28.10.17.s19.
Edwards syndrome: Neurocognitive and linguistic profile, diagnosis, overlaps and treatment.
Katsarou DV, Argyriadis A, Sofologi M, Argyriadi A, Kougioumtzis GA, Megari K, Mantsos E, Theodoratou M.
Pol Merkur Lekarski. 2025;53(4):540-545. doi: 10.36740/Merkur202504116.
Double trisomy 48,XXX,+18 with multiple dysmorphic features.
Jiang ZY, Wu XH, Zou CC.
World J Pediatr. 2015 Feb;11(1):83-8. doi: 10.1007/s12519-015-0005-7. Epub 2015 Jan 28.
Surveillance guidelines for children with trisomy 18.
Kepple JW, Fishler KP, Peeples ES.
Am J Med Genet A. 2021 Apr;185(4):1294-1303. doi: 10.1002/ajmg.a.62097. Epub 2021 Feb 2.
[Trisomy 18 syndrome: A case report].
Saldarriaga W, Rengifo-Miranda H, Ramírez-Cheyne J.
Rev Chil Pediatr. 2016 Mar-Apr;87(2):129-36. doi: 10.1016/j.rchipe.2015.08.006. Epub 2015 Oct 12.
A tumor profile in Edwards syndrome (trisomy 18).
Satgé D, Nishi M, Sirvent N, Vekemans M.
Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):296-306. doi: 10.1002/ajmg.c.31511. Epub 2016 Jul 30.
A rare case report of Edwards syndrome with immature teratoma in submandibular region and literature review.
Gerakova E, Genova S.
Folia Med (Plovdiv). 2022 Apr 30;64(2):348-353. doi: 10.3897/folmed.64.e61024.
[Trisomy 18 or postnatal Edward s syndrome: descriptive study conducted at the University Hospital Center of Casablanca and literature review].
Outtaleb FZ, Errahli R, Imelloul N, Jabrane G, Serbati N, Dehbi H.
Pan Afr Med J. 2020 Dec 3;37:309. doi: 10.11604/pamj.2020.37.309.26205. eCollection 2020.
Trisomies.
Levy PA, Marion R.
Pediatr Rev. 2018 Feb;39(2):104-106. doi: 10.1542/pir.2016-0198.
Prolonged survival in Edwards syndrome with congenital heart disease: a case report and literature review.
López-Ríos V, Grajales-Marín E, Gómez-Zambrano V, Barrios-Arroyave FA.
Medwave. 2020 Sep 3;20(8):e8015. doi: 10.5867/medwave.2020.08.8015.
