Literature DB >> 12755177

Do children with myelomeningocele and hydrocephalus display nonverbal learning disabilities? An empirical approach to classification.

Keith Owen Yeates1, Nancy Loss, Andrew N Colvin, Benedicta G Enrile.   

Abstract

As a group, children with myelomeningocele (MM) and early-onset hydrocephalus demonstrate many of the features of the syndrome of nonverbal learning disabilities (NLD). However, the frequency with which individual children display a pattern of neuropsychological functioning consistent with the NLD syndrome is unknown. We addressed this question by comparing the prevalence of NLD in 32 children with MM and shunted hydrocephalus to that in a group of 27 healthy siblings. Participants, who were between 8 and 15 years of age, completed a neuropsychological test battery that included 11 measures of possible assets and 17 measures of possible deficits that define the NLD syndrome. As a group, children with MM and shunted hydrocephalus displayed many of the specific assets and deficits. However, they also displayed significantly more variability in their patterns of assets and deficits than siblings, reflecting the substantial individual differences that characterize children with MM. About 50% of the children with myelomeningocele displayed a pattern of assets and deficits consistent with the NLD syndrome. Classification as NLD was weakly related to cumulative medical risk, as well as to left-handedness. The findings suggest a need for caution in making generalizations regarding the applicability of the NLD model to children with MM and early-onset hydrocephalus.

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Year:  2003        PMID: 12755177     DOI: 10.1017/S1355617703940057

Source DB:  PubMed          Journal:  J Int Neuropsychol Soc        ISSN: 1355-6177            Impact factor:   2.892


  7 in total

1.  Gray matter integrity within regions of the dorsolateral prefrontal cortical-subcortical network predicts executive function and fine motor dexterity in spina bifida.

Authors:  Ashley L Ware; Paulina A Kulesz; Victoria J Williams; Jenifer Juranek; Paul T Cirino; Jack M Fletcher
Journal:  Neuropsychology       Date:  2016-01-11       Impact factor: 3.295

2.  A comparison of the MOMS trial results to a contemporaneous, single-institution, postnatal closure cohort.

Authors:  Nicholas M B Laskay; Anastasia A Arynchyna; Samuel G McClugage; Betsy Hopson; Chevis Shannon; Benjamin Ditty; John C Wellons; Jeffrey P Blount; Brandon G Rocque
Journal:  Childs Nerv Syst       Date:  2016-12-27       Impact factor: 1.475

3.  Profiles of Neuropsychological Functioning in Children and Adolescents with Spina Bifida: Associations with Biopsychosocial Predictors and Functional Outcomes.

Authors:  Rachel M Wasserman; Grayson N Holmbeck
Journal:  J Int Neuropsychol Soc       Date:  2016-08-30       Impact factor: 2.892

4.  Morphological and behavioral changes in the pathogenesis of a novel mouse model of communicating hydrocephalus.

Authors:  Allison B McMullen; Gurlal S Baidwan; Ken D McCarthy
Journal:  PLoS One       Date:  2012-01-24       Impact factor: 3.240

5.  Pain and health status in adults with myelomeningocele living in Sweden.

Authors:  Ann Alriksson-Schmidt; Annika Lundkvist Josenby; Barbro Lindquist; Lena Westbom
Journal:  J Pediatr Rehabil Med       Date:  2018

6.  Pressure injuries are common in children with myelomeningocele: Results from a follow-up programme and register.

Authors:  Jessica Stockman; Lena Westbom; Ann I Alriksson-Schmidt
Journal:  Acta Paediatr       Date:  2022-05-27       Impact factor: 4.056

7.  The natural history of spina bifida in children pilot project: research protocol.

Authors:  Ann I Alriksson-Schmidt; Judy K Thibadeau; Mark E Swanson; David Marcus; Kari L Carris; Csaba Siffel; Elisabeth Ward
Journal:  JMIR Res Protoc       Date:  2013-01-25
  7 in total

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