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Twenty\u2010seven subjects of age 16\u201325 with juvenile DM1 and their parents were invited to have a clinical psychiatric interview, and to complete an ASEBA behavior checklist (YSR, ASR, CBCL, and ABCL). We diagnosed a Delusional Disorder in 19% of our patients and a Psychotic Disorder not otherwise specified in another 19%. These two groups of patients had a significantly worse level of clinically defined general functioning. It is clinically relevant to investigate in patients with juvenile DM the symptom of delusions and the presence of a delusional and psychotic disorder, and to consider the presence of juvenile DM in youngsters presenting with such a thought disorder. These disorders compromise the general functioning of the subjects and are often to some extent treatable. \u00a9 2017 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.b.32524","type":"journal-article","created":{"date-parts":[[2017,4,27]],"date-time":"2017-04-27T23:41:27Z","timestamp":1493336487000},"page":"359-366","source":"Crossref","is-referenced-by-count":5,"title":["Delusional and psychotic disorders in juvenile myotonic dystrophy type\u20101"],"prefix":"10.1002","volume":"174","author":[{"given":"Delphine","family":"Jacobs","sequence":"first","affiliation":[{"name":"Centre for Human Genetics University of Leuven Leuven Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Diane","family":"Willekens","sequence":"additional","affiliation":[{"name":"Centre for Human Genetics University of Leuven Leuven Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christine","family":"de Die\u2010Smulders","sequence":"additional","affiliation":[{"name":"Department of Clinical Genetics Academic Hospital Maastricht Maastricht The Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean\u2010Pierre","family":"Frijns","sequence":"additional","affiliation":[{"name":"Centre for Human Genetics University of Leuven Leuven Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean","family":"Steyaert","sequence":"additional","affiliation":[{"name":"Centre for Human Genetics University of Leuven Leuven Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,4,27]]},"reference":[{"key":"e_1_2_7_2_1","volume-title":"Manual for the ASEBA School\u2010Age Forms & Profiles","author":"Achenbach T","year":"2001"},{"key":"e_1_2_7_3_1","volume-title":"Manual for the ASEBA Adult Forms & Profiles","author":"Achenbach T","year":"2003"},{"key":"e_1_2_7_4_1","volume-title":"Diagnostic and Statistical Manual of Mental Disorders, 4th edition, Text Revision (DSM\u2010IV\u2010TR), 4e","year":"2000"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.nmd.2007.02.012"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1080\/16501970500477967"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0092-8674(92)90154-5"},{"key":"e_1_2_7_8_1","doi-asserted-by":"publisher","DOI":"10.2466\/pr0.1987.60.3.783"},{"key":"e_1_2_7_9_1","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp.65.3.353"},{"key":"e_1_2_7_10_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00314629"},{"key":"e_1_2_7_11_1","doi-asserted-by":"publisher","DOI":"10.1192\/bjp.169.1.58"},{"key":"e_1_2_7_12_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0960-8966(99)00055-3"},{"key":"e_1_2_7_13_1","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1093\/oso\/9780198527824.003.0014","volume-title":"Congenital and childhood\u2010onset myotonic dystrophy. 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