{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T11:07:43Z","timestamp":1780916863116,"version":"3.54.1"},"reference-count":51,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2020,2,14]],"date-time":"2020-02-14T00:00:00Z","timestamp":1581638400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2020,2,14]],"date-time":"2020-02-14T00:00:00Z","timestamp":1581638400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Molec Gen &amp;amp; Gen Med"],"published-print":{"date-parts":[[2020,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Noonan Syndrome is a developmental disorder characterized by a distinctive phenotype including facial dysmorphism, webbed neck, short stature, heart defects, and variable cognitive deficits as major features. Over the years, neuropsychological and behavioral studies explored alteration of cognitive functioning and related domains, such as learning, memory, and attention. To our knowledge, however, data concerning the language profile in this disorder is scarce. The aim of the present study was to detect specific language functioning combining nonverbal intelligence quotient and language abilities and to pinpoint strengths and weaknesses in the language domains.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>The language profile of 37 Italian participants with molecularly confirmed diagnosis of Noonan Syndrome was evaluated using specific tools to assess vocabulary and grammar comprehension and production, as well as phonological development.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>We observed that 78% of affected individuals exhibited language impairment. Within language domains, the strong area was lexical production and grammar production was the weak area. Almost half the participants manifested a similar trend of specific language impairment. Nonverbal intelligence quotient only correlated with grammar comprehension.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Our study expands present knowledge about the language profile in NS, and provides data that could enable more effective patient management and appropriate intervention.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/mgg3.1069","type":"journal-article","created":{"date-parts":[[2020,2,14]],"date-time":"2020-02-14T13:40:10Z","timestamp":1581687610000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Defining language disorders in children and adolescents with Noonan Syndrome"],"prefix":"10.1002","volume":"8","author":[{"given":"Giulia","family":"Lazzaro","sequence":"first","affiliation":[{"name":"Department of Neuroscience, Child and Adolescent Psychiatric Unit Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"},{"name":"Department of Human Science LUMSA University of Rome Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cristina","family":"Caciolo","sequence":"additional","affiliation":[{"name":"Department of Neuroscience, Child and Adolescent Psychiatric Unit Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Deny","family":"Menghini","sequence":"additional","affiliation":[{"name":"Department of Neuroscience, Child and Adolescent Psychiatric Unit Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francesca","family":"Cumbo","sequence":"additional","affiliation":[{"name":"Department of Neuroscience, Child and Adolescent Psychiatric Unit Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria C.","family":"Digilio","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rossella","family":"Capolino","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics Bambino Ges\u00f9 Children\u2019s Hospital IRCCS Rome Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Giuseppe","family":"Zampino","sequence":"additional","affiliation":[{"name":"Center for Rare Disease and Congenital Defects Fondazione Policlinico Universitario A. 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