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We report a 19p13.13 microdeletion, detected by array CGH, in a girl with moderate intellectual disability, overgrowth with macrocephaly, prominent digit pads and deep digital creases, hypotonia, ataxia, and strabismus. This clinical report helps to delineate the role of some of the deleted genes, as well as the phenotype of recently described 19p13.13 microdeletion syndrome, including the description of novel digital abnormalities. \u00a9 2015 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.37280","type":"journal-article","created":{"date-parts":[[2015,9,4]],"date-time":"2015-09-04T06:45:14Z","timestamp":1441349114000},"page":"2839-2843","source":"Crossref","is-referenced-by-count":8,"title":["Intellectual disability and overgrowth\u2014A new case of 19p13.13 microdeletion syndrome with digital abnormalities"],"prefix":"10.1002","volume":"167","author":[{"given":"Rita","family":"Jorge","sequence":"first","affiliation":[{"name":"Department of Paediatrics S\u00e3o Jo\u00e3o Hospital Centre Porto Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carmen","family":"Silva","sequence":"additional","affiliation":[{"name":"Department of Paediatrics S\u00e3o 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