{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,12]],"date-time":"2025-10-12T20:09:31Z","timestamp":1760299771746},"reference-count":16,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2018,1,4]],"date-time":"2018-01-04T00:00:00Z","timestamp":1515024000000},"content-version":"vor","delay-in-days":3,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Special Care in Dentistry"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>We described herein the oral and craniofacial features of a 7\u2010year\u2010old boy, diagnosed <jats:italic>in utero<\/jats:italic> with mucopolysaccharidosis II (MPS II), who was treated with hematopoietic stem cell transplantation (HSCT) at 70 days of age. The main oral clinical findings were the following: macroglossia, posterior cross\u2010bite, crowding, pointed cuspid teeth, delayed tooth eruption, retained primary teeth, and enamel hypoplasia. The image examination showed: retention eruption, posterior primary teeth with short roots, absence of some permanent teeth, and stretching of the stylohyoid processes bilaterally. This patient showed the importance of early diagnosis and HSCT therapy in attenuating the clinical and radiographic oral and craniofacial manifestations of the MPS II patient.<\/jats:p>","DOI":"10.1111\/scd.12260","type":"journal-article","created":{"date-parts":[[2018,1,4]],"date-time":"2018-01-04T12:32:35Z","timestamp":1515069155000},"page":"51-54","source":"Crossref","is-referenced-by-count":7,"title":["Oral and craniofacial manifestations in a Hunter syndrome patient with hematopoietic stem cell transplantation: A case report"],"prefix":"10.1111","volume":"38","author":[{"given":"Rafaela de Oliveira","family":"Torres","sequence":"first","affiliation":[{"name":"Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andr\u00e9a Vaz Braga","family":"Pintor","sequence":"additional","affiliation":[{"name":"Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F\u00e1bio Ribeiro","family":"Guedes","sequence":"additional","affiliation":[{"name":"Department of Oral Pathology Universidade Federal do Rio de Janeiro  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Liana Bastos","family":"Freitas\u2010Fernandes","sequence":"additional","affiliation":[{"name":"Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anneliese Lopes","family":"Barth","sequence":"additional","affiliation":[{"name":"Department of Genetics Instituto Fernandes Figueira  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dafne Dain Gandelman","family":"Horovitz","sequence":"additional","affiliation":[{"name":"Department of Genetics Instituto Fernandes Figueira  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ivete Pomarico Ribeiro","family":"de Souza","sequence":"additional","affiliation":[{"name":"Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro  Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2018,1,4]]},"reference":[{"key":"e_1_2_6_2_1","first-page":"26","article-title":"Management of the behavioural manifestations of Hunter syndrome","volume":"25","author":"Roberts J","year":"2010","journal-title":"Br J Nurs"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1038\/sj.bmt.1703839"},{"key":"e_1_2_6_4_1","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1007\/s12687-015-0230-8","article-title":"The Latin American School of Human and Medical Genetics: promoting education and collaboration in genetics and ethics applied to health sciences across the continent","volume":"6","author":"Giugliani R","year":"2015","journal-title":"J Community Genet"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1590\/S1415-47572014000300003"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.3109\/00016357.2011.654255"},{"key":"e_1_2_6_7_1","doi-asserted-by":"crossref","first-page":"66","DOI":"10.4103\/0970-4388.149011","article-title":"NS Hunter's syndrome: a case report","volume":"33","author":"Savitha NS","year":"2015","journal-title":"J Indian Soc Pedod Prev Dent"},{"key":"e_1_2_6_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bbmt.2016.08.015"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymgmr.2017.05.010"},{"key":"e_1_2_6_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jpeds.2008.11.041"},{"key":"e_1_2_6_11_1","first-page":"487","article-title":"Hunter syndrome (Mucopolysaccharidosis type II), severe phenotype: long term follow\u2010up on patients undergone to hematopoietic stem cell transplantation","volume":"65","author":"Annibali R","year":"2013","journal-title":"Minerva Pediatr"},{"key":"e_1_2_6_12_1","doi-asserted-by":"publisher","DOI":"10.1038\/sj.bmt.1702397"},{"key":"e_1_2_6_13_1","first-page":"1993","volume-title":"Mucopolysaccharidosis Type II. 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