Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression
Objective: To evaluate the cognitive profiles of children with Noonan syndrome (NS) and to relate these profiles to measures of overall clinical severity. Study design: Thirty-five children with NS between the ages of 7 and 18 years were tested on their intellectual, psychosocial, and academic funct...
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Veröffentlicht in: | The Journal of pediatrics 1999-12, Vol.135 (6), p.707-713 |
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description | Objective: To evaluate the cognitive profiles of children with Noonan syndrome (NS) and to relate these profiles to measures of overall clinical severity.
Study design: Thirty-five children with NS between the ages of 7 and 18 years were tested on their intellectual, psychosocial, and academic functioning. The diagnosis of NS was established on the presence of a typical face, the characteristic heart defect, thorax deformity, short stature, affected first-degree relative(s), and cryptorchidism in male subjects.
Results: The total group of children with NS (n = 35) achieved significantly lower mean full-scale IQ, verbal IQ (VIQ), and performance IQ (PIQ) scores (between 85.9 and 89.3) than expected based on normative data. The individual full-scale IQ scores varied between 48 and 130. Because of this wide range of individual scores, the mean group values are not extremely informative. The mean full-scale IQ for the group with moderate NS (n = 19) is 90.8; for the children with severe NS (n = 16) the mean full-scale IQ is 80.6. The patterns of discrepancies between VIQ and PIQ are: (1) an extreme discrepancy between VIQ and PIQ is most likely to emerge in children with severe NS with (low) average intellectual abilities; (2) children with moderate NS are more likely to attain similarities in VIQ and PIQ scores; and (3) children with moderate NS demonstrate a particular pattern of discrepancy between VIQ and PIQ (ie, VIQ > PIQ).
Conclusion: For children with NS, the findings on physical examination are indicative of the pattern of cognitive abilities. NS is not associated with substantial deficits in the level of intellectual functioning or with a single/unitary cognitive pattern. Severe NS expression, however, predicts in part a specific pattern of deficits and capacities in cognitive functioning. (J Pediatr 1999;135:707-13) |
doi_str_mv | 10.1016/S0022-3476(99)70089-2 |
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Study design: Thirty-five children with NS between the ages of 7 and 18 years were tested on their intellectual, psychosocial, and academic functioning. The diagnosis of NS was established on the presence of a typical face, the characteristic heart defect, thorax deformity, short stature, affected first-degree relative(s), and cryptorchidism in male subjects.
Results: The total group of children with NS (n = 35) achieved significantly lower mean full-scale IQ, verbal IQ (VIQ), and performance IQ (PIQ) scores (between 85.9 and 89.3) than expected based on normative data. The individual full-scale IQ scores varied between 48 and 130. Because of this wide range of individual scores, the mean group values are not extremely informative. The mean full-scale IQ for the group with moderate NS (n = 19) is 90.8; for the children with severe NS (n = 16) the mean full-scale IQ is 80.6. The patterns of discrepancies between VIQ and PIQ are: (1) an extreme discrepancy between VIQ and PIQ is most likely to emerge in children with severe NS with (low) average intellectual abilities; (2) children with moderate NS are more likely to attain similarities in VIQ and PIQ scores; and (3) children with moderate NS demonstrate a particular pattern of discrepancy between VIQ and PIQ (ie, VIQ > PIQ).
Conclusion: For children with NS, the findings on physical examination are indicative of the pattern of cognitive abilities. NS is not associated with substantial deficits in the level of intellectual functioning or with a single/unitary cognitive pattern. Severe NS expression, however, predicts in part a specific pattern of deficits and capacities in cognitive functioning. (J Pediatr 1999;135:707-13)</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/S0022-3476(99)70089-2</identifier><identifier>PMID: 10586173</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; Chromosome aberrations ; Cognition ; Female ; Humans ; Intelligence ; Intelligence Tests ; Male ; Medical genetics ; Medical sciences ; Noonan Syndrome ; Phenotype ; Severity of Illness Index</subject><ispartof>The Journal of pediatrics, 1999-12, Vol.135 (6), p.707-713</ispartof><rights>1999 Mosby, Inc.</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-3bde355051db2f923f84233677f97494f0d1bea716666fd8023a621b33b47b933</citedby><cites>FETCH-LOGICAL-c442t-3bde355051db2f923f84233677f97494f0d1bea716666fd8023a621b33b47b933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022347699700892$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1263869$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10586173$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Burgt, Ineke</creatorcontrib><creatorcontrib>Thoonen, Geert</creatorcontrib><creatorcontrib>Roosenboom, Natasja</creatorcontrib><creatorcontrib>Assman-Hulsmans, Claire</creatorcontrib><creatorcontrib>Gabreels, Fons</creatorcontrib><creatorcontrib>Otten, Barto</creatorcontrib><creatorcontrib>Brunner, Han G.</creatorcontrib><title>Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><description>Objective: To evaluate the cognitive profiles of children with Noonan syndrome (NS) and to relate these profiles to measures of overall clinical severity.
Study design: Thirty-five children with NS between the ages of 7 and 18 years were tested on their intellectual, psychosocial, and academic functioning. The diagnosis of NS was established on the presence of a typical face, the characteristic heart defect, thorax deformity, short stature, affected first-degree relative(s), and cryptorchidism in male subjects.
Results: The total group of children with NS (n = 35) achieved significantly lower mean full-scale IQ, verbal IQ (VIQ), and performance IQ (PIQ) scores (between 85.9 and 89.3) than expected based on normative data. The individual full-scale IQ scores varied between 48 and 130. Because of this wide range of individual scores, the mean group values are not extremely informative. The mean full-scale IQ for the group with moderate NS (n = 19) is 90.8; for the children with severe NS (n = 16) the mean full-scale IQ is 80.6. The patterns of discrepancies between VIQ and PIQ are: (1) an extreme discrepancy between VIQ and PIQ is most likely to emerge in children with severe NS with (low) average intellectual abilities; (2) children with moderate NS are more likely to attain similarities in VIQ and PIQ scores; and (3) children with moderate NS demonstrate a particular pattern of discrepancy between VIQ and PIQ (ie, VIQ > PIQ).
Conclusion: For children with NS, the findings on physical examination are indicative of the pattern of cognitive abilities. NS is not associated with substantial deficits in the level of intellectual functioning or with a single/unitary cognitive pattern. Severe NS expression, however, predicts in part a specific pattern of deficits and capacities in cognitive functioning. (J Pediatr 1999;135:707-13)</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Chromosome aberrations</subject><subject>Cognition</subject><subject>Female</subject><subject>Humans</subject><subject>Intelligence</subject><subject>Intelligence Tests</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Noonan Syndrome</subject><subject>Phenotype</subject><subject>Severity of Illness Index</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEuvEzEMRiME4pbCTwBlgRAsBvKYmUxWCF3xkq4ACVhHmcRpjaZJSdJC1_xxpg8BO7zxwsf2p0PIQ86ec8b7F58ZE6KRreqfav1MMTboRtwiC860avpByttk8Qe5IvdK-cYY0y1jd8kVZ93QcyUX5NcnWyvkWGgK1KVVxIp7oGEXXcUUMa4oRlrcOqWpsSvw1K1x8hki_YF1TT-kFO0MHKLPaQPUlpIc2jqDp_neZrQjTlgPx0PbNcRUD1t0FH5uM5QyP7lP7gQ7FXhw6Uvy9c3rL9fvmpuPb99fv7ppXNuK2sjRg-w61nE_iqCFDEMrpOyVClq1ug3M8xGs4v1cwQ9MSNsLPko5tmrUUi7Jk_PdbU7fd1Cq2WBxME02QtoV08-MkuIIdmfQ5VRKhmC2GTc2Hwxn5mjfnOybo1qjtTnZN2Lee3R5sBs34P_ZOuuegccXwBZnp5BtdFj-cqKXw5xiSV6eMZht7BGyKQ4hOvCYwVXjE_4nyW8U0qOZ</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>van der Burgt, Ineke</creator><creator>Thoonen, Geert</creator><creator>Roosenboom, Natasja</creator><creator>Assman-Hulsmans, Claire</creator><creator>Gabreels, Fons</creator><creator>Otten, Barto</creator><creator>Brunner, Han G.</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19991201</creationdate><title>Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression</title><author>van der Burgt, Ineke ; Thoonen, Geert ; Roosenboom, Natasja ; Assman-Hulsmans, Claire ; Gabreels, Fons ; Otten, Barto ; Brunner, Han G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-3bde355051db2f923f84233677f97494f0d1bea716666fd8023a621b33b47b933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Chromosome aberrations</topic><topic>Cognition</topic><topic>Female</topic><topic>Humans</topic><topic>Intelligence</topic><topic>Intelligence Tests</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Noonan Syndrome</topic><topic>Phenotype</topic><topic>Severity of Illness Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Burgt, Ineke</creatorcontrib><creatorcontrib>Thoonen, Geert</creatorcontrib><creatorcontrib>Roosenboom, Natasja</creatorcontrib><creatorcontrib>Assman-Hulsmans, Claire</creatorcontrib><creatorcontrib>Gabreels, Fons</creatorcontrib><creatorcontrib>Otten, Barto</creatorcontrib><creatorcontrib>Brunner, Han G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Burgt, Ineke</au><au>Thoonen, Geert</au><au>Roosenboom, Natasja</au><au>Assman-Hulsmans, Claire</au><au>Gabreels, Fons</au><au>Otten, Barto</au><au>Brunner, Han G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>1999-12-01</date><risdate>1999</risdate><volume>135</volume><issue>6</issue><spage>707</spage><epage>713</epage><pages>707-713</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>Objective: To evaluate the cognitive profiles of children with Noonan syndrome (NS) and to relate these profiles to measures of overall clinical severity.
Study design: Thirty-five children with NS between the ages of 7 and 18 years were tested on their intellectual, psychosocial, and academic functioning. The diagnosis of NS was established on the presence of a typical face, the characteristic heart defect, thorax deformity, short stature, affected first-degree relative(s), and cryptorchidism in male subjects.
Results: The total group of children with NS (n = 35) achieved significantly lower mean full-scale IQ, verbal IQ (VIQ), and performance IQ (PIQ) scores (between 85.9 and 89.3) than expected based on normative data. The individual full-scale IQ scores varied between 48 and 130. Because of this wide range of individual scores, the mean group values are not extremely informative. The mean full-scale IQ for the group with moderate NS (n = 19) is 90.8; for the children with severe NS (n = 16) the mean full-scale IQ is 80.6. The patterns of discrepancies between VIQ and PIQ are: (1) an extreme discrepancy between VIQ and PIQ is most likely to emerge in children with severe NS with (low) average intellectual abilities; (2) children with moderate NS are more likely to attain similarities in VIQ and PIQ scores; and (3) children with moderate NS demonstrate a particular pattern of discrepancy between VIQ and PIQ (ie, VIQ > PIQ).
Conclusion: For children with NS, the findings on physical examination are indicative of the pattern of cognitive abilities. NS is not associated with substantial deficits in the level of intellectual functioning or with a single/unitary cognitive pattern. Severe NS expression, however, predicts in part a specific pattern of deficits and capacities in cognitive functioning. (J Pediatr 1999;135:707-13)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>10586173</pmid><doi>10.1016/S0022-3476(99)70089-2</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Child Chromosome aberrations Cognition Female Humans Intelligence Intelligence Tests Male Medical genetics Medical sciences Noonan Syndrome Phenotype Severity of Illness Index |
title | Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression |
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