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Patients are often initially misdiagnosed as having idiopathic developmental delay, attention deficit\/hyperactivity disorder and\/or autism spectrum disorders, putting them at risk for unnecessary testing and treatments.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Children with developmental or speech delay, especially those with a characteristic somatic feature or behavioural abnormalities, should be screened for <jats:styled-content style=\"fixed-case\">MPS III<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/apa.12169","type":"journal-article","created":{"date-parts":[[2013,1,21]],"date-time":"2013-01-21T14:17:56Z","timestamp":1358777876000},"page":"462-470","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":121,"title":["Mucopolysaccharidosis type <scp>III<\/scp> (<scp>S<\/scp>anfilippo syndrome) and misdiagnosis of idiopathic developmental delay, attention deficit\/hyperactivity disorder or autism spectrum disorder"],"prefix":"10.1111","volume":"102","author":[{"given":"Frits A","family":"Wijburg","sequence":"first","affiliation":[{"name":"Department of Paediatrics Academic Medical Centre Amsterdam The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Grzegorz","family":"W\u0119grzyn","sequence":"additional","affiliation":[{"name":"Department of Molecular Biology University of Gda\u0144sk Gda\u0144sk Poland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Barbara K","family":"Burton","sequence":"additional","affiliation":[{"name":"Division of Genetics, Birth Defects and Metabolism Ann &amp; Robert H. 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