Literature DB >> 11738354

Intelligence and cognitive function in children and adolescents with spinal muscular atrophy.

A von Gontard1, K Zerres, M Backes, C Laufersweiler-Plass, C Wendland, P Melchers, G Lehmkuhl, S Rudnik-Schöneborn.   

Abstract

Spinal muscular atrophy is a chronic disease characterised by loss of motor function. The aim of the study was to analyse cognitive functions in a large group of patients with spinal muscular atrophy. It was hypothesised that their intelligence is comparable to controls, but not above average as previously postulated. Ninety-six children and adolescents with spinal muscular atrophy I-III, aged 6.0-18.11 years, 45 non-affected siblings and 59 healthy, matched controls were examined with one- (CPM/SPM), as well as multi-dimensional intelligence tests (Kaufman-ABC; Wechsler tests). The mean IQ measured with the CPM/SPM tests was 109.6 for the spinal muscular atrophy group, 107.3 for the sibs and 104.1 for the healthy controls (no significant difference). In the older children and adolescents (SPM only) the mean IQ was significantly higher for the spinal muscular atrophy patients (109.6) than for the controls (95.4). The standard score in the 'mental processing composite' scale of the Kaufman-ABC was identical in the spinal muscular atrophy group and controls (103.8). The cognitive profile was relatively homogeneous. However, the older children and adolescents did have a significantly higher verbal IQ (113.8) than controls (104.6) in the Wechsler tests. There were no significant differences in any of the tests among different grades of severity (spinal muscular atrophy types I-III). It can be concluded that children and adolescents with spinal muscular atrophy have a general intelligence in the normal range. By adolescence, environmentally mediated aspects of intelligence are higher in patients with spinal muscular atrophy. It could be speculated that the development of cognitive skills and knowledge is a creative way to compensate the many restrictions due to their physical handicap.

Entities:  

Mesh:

Year:  2002        PMID: 11738354     DOI: 10.1016/s0960-8966(01)00274-7

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  17 in total

Review 1.  Spinal Muscular Atrophy.

Authors:  Stephen J Kolb; John T Kissel
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

Review 2.  Spinal muscular atrophy: diagnosis and management in a new therapeutic era.

Authors:  W David Arnold; Darine Kassar; John T Kissel
Journal:  Muscle Nerve       Date:  2014-12-16       Impact factor: 3.217

3.  Current Status of the Utilization of Powered Wheelchair in Preschool Children with Locomotive Disability in Japan.

Authors:  Sachie Uyama; Keiichi Hanaki
Journal:  Phys Ther Res       Date:  2016-07-15

4.  Review of Spinal Muscular Atrophy (SMA) for Prenatal and Pediatric Genetic Counselors.

Authors:  Amanda Carré; Candice Empey
Journal:  J Genet Couns       Date:  2015-08-08       Impact factor: 2.537

Review 5.  Spinal muscular atrophy: a motor neuron disorder or a multi-organ disease?

Authors:  Monir Shababi; Christian L Lorson; Sabine S Rudnik-Schöneborn
Journal:  J Anat       Date:  2013-07-22       Impact factor: 2.610

Review 6.  Urinary incontinence in children with special needs.

Authors:  Alexander von Gontard
Journal:  Nat Rev Urol       Date:  2013-10-01       Impact factor: 14.432

Review 7.  Proximal spinal muscular atrophy: current orthopedic perspective.

Authors:  Gerrit Haaker; Albert Fujak
Journal:  Appl Clin Genet       Date:  2013-11-14

8.  Functional Abnormalities of Cerebellum and Motor Cortex in Spinal Muscular Atrophy Mice.

Authors:  Arumugarajah Tharaneetharan; Madison Cole; Brandon Norman; Nayeli C Romero; Julian R A Wooltorton; Melissa A Harrington; Jianli Sun
Journal:  Neuroscience       Date:  2020-11-17       Impact factor: 3.590

Review 9.  Self-locomotion and spatial language and spatial cognition: insights from typical and atypical development.

Authors:  Ora Oudgenoeg-Paz; James Rivière
Journal:  Front Psychol       Date:  2014-06-02

10.  Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study.

Authors:  Ying Qian; Sarah McGraw; Jeff Henne; Jill Jarecki; Kenneth Hobby; Wei-Shi Yeh
Journal:  BMC Neurol       Date:  2015-10-24       Impact factor: 2.474

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.