Literature DB >> 3810072

Autism and genetic disorders.

A L Reiss, C Feinstein, K N Rosenbaum.   

Abstract

The syndrome of autism has been documented as occurring in association with a wide variety of genetic conditions. Autistic patients with a coexistent genetic condition, however, are not behaviorally or developmentally distinct from autistic patients for whom there is no known etiology or associated organic condition. This report reviews the literature linking autistic behavior with genetic conditions. Genetic, neurodevelopmental, and neuropathological findings in three genetic conditions which frequently give rise to autism are presented in detail. On the basis of this review, two hypotheses are supported: autism is a behaviorally defined phenotype which arises from diverse causes of central nervous system (CNS) damage, and the autistic phenotype represents only one point along a continuum of psychological dysfunction resulting from CNS damage. Current theories of genetic influences on brain development are reviewed, with emphasis on the relationships among qualitative, quantitative, and temporal abnormalities of CNS maturation and behavioral dysfunction. A hypothesis of abnormal brain development resulting from dysfunctional myelination is proposed as a potential etiologic factor in autism.

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Year:  1986        PMID: 3810072     DOI: 10.1093/schbul/12.4.724

Source DB:  PubMed          Journal:  Schizophr Bull        ISSN: 0586-7614            Impact factor:   9.306


  10 in total

Review 1.  Classification of pervasive developmental disorders: some concepts and practical considerations.

Authors:  M Rutter; E Schopler
Journal:  J Autism Dev Disord       Date:  1992-12

2.  Parental inheritance and psychological disability in fragile X females.

Authors:  A L Reiss; L Freund; S Vinogradov; R Hagerman; A Cronister
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

3.  Family history of cognitive disabilities in first-degree relatives of autistic and mentally retarded children.

Authors:  P Boutin; M Maziade; C Mérette; M Mondor; C Bédard; J Thivierge
Journal:  J Autism Dev Disord       Date:  1997-04

4.  Autism associated with tetrasomy 15: A further report.

Authors:  Mohammad Ghaziuddin; Susan Sheldon; Sanjiv Venkataraman; Luke Tsai; Neera Ghaziuddin
Journal:  Eur Child Adolesc Psychiatry       Date:  1993-10       Impact factor: 4.785

5.  Autism and tuberous sclerosis.

Authors:  S L Smalley; P E Tanguay; M Smith; G Gutierrez
Journal:  J Autism Dev Disord       Date:  1992-09

6.  Autism and phenylketonuria.

Authors:  Sabrina Baieli; Lorenzo Pavone; Concetta Meli; Agata Fiumara; Mary Coleman
Journal:  J Autism Dev Disord       Date:  2003-04

Review 7.  Human pluripotent stem cell models of Fragile X syndrome.

Authors:  Anita Bhattacharyya; Xinyu Zhao
Journal:  Mol Cell Neurosci       Date:  2015-11-27       Impact factor: 4.314

8.  Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells.

Authors:  Meng Li; Huashan Zhao; Gene E Ananiev; Michael T Musser; Kathryn H Ness; Dianne L Maglaque; Krishanu Saha; Anita Bhattacharyya; Xinyu Zhao
Journal:  Stem Cells       Date:  2016-07-27       Impact factor: 6.277

9.  Genetics and mitochondrial abnormalities in autism spectrum disorders: a review.

Authors:  Sukhbir Dhillon; Jessica A Hellings; Merlin G Butler
Journal:  Curr Genomics       Date:  2011-08       Impact factor: 2.236

10.  MAPK3 at the Autism-Linked Human 16p11.2 Locus Influences Precise Synaptic Target Selection at Drosophila Larval Neuromuscular Junctions.

Authors:  Sang Mee Park; Hae Ryoun Park; Ji Hye Lee
Journal:  Mol Cells       Date:  2017-02-15       Impact factor: 5.034

  10 in total

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