Literature DB >> 3198900

Cognitive profile of Rett syndrome.

J Fontanesi1, R H Haas.   

Abstract

We report preliminary studies in 18 girls with Rett syndrome (15 typical, three atypical cases) who were studied using a number of neuropsychologic measures. Results indicate a relative preservation of gross motor and daily living skills at the developmental level of the age of onset of the condition. Other adaptive functions were more depressed. Higher levels of object permanency were found in this population than reported previously. Our results indicate that islands of motor and intellectual function persist in Rett syndrome patients. These data may be useful for therapeutic intervention.

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Year:  1988        PMID: 3198900     DOI: 10.1177/0883073888003001s05

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  4 in total

1.  Describing the phenotype in Rett syndrome using a population database.

Authors:  L Colvin; S Fyfe; S Leonard; T Schiavello; C Ellaway; N De Klerk; J Christodoulou; M Msall; H Leonard
Journal:  Arch Dis Child       Date:  2003-01       Impact factor: 3.791

Review 2.  Rett syndrome: a review of current knowledge.

Authors:  R Van Acker
Journal:  J Autism Dev Disord       Date:  1991-12

3.  Brief report: cognitive and adaptive functioning in 28 girls with Rett syndrome.

Authors:  A Perry; N Sarlo-McGarvey; C Haddad
Journal:  J Autism Dev Disord       Date:  1991-12

4.  Caregiver- and Clinician-Reported Adaptive Functioning in Rett Syndrome: a Systematic Review and Evaluation of Measurement Strategies.

Authors:  Eric S Semmel; Michelle E Fox; Sabrina D Na; Rella Kautiainen; Robert D Latzman; Tricia Z King
Journal:  Neuropsychol Rev       Date:  2019-11-20       Impact factor: 7.444

  4 in total

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