Literature DB >> 8463065

The neurobiology and genetics of infantile autism.

L J Lotspeich1, R D Ciaranello.   

Abstract

Autism is a syndrome with multiple etiologies, as is made clear both by the evidence of neurobiological research and by the catalog of disorders that present with autistic behaviors. What remains unclear are the specific neuropathological mechanisms that produce autistic behaviors; for example, is there a common neuroanatomic pathology for all cases of autism, or can autistic behaviors emerge from different pathological sequences within the brain? Although it is premature to generalize, neuropathological studies appear to have identified common abnormalities in the cerebellum and limbic system of at least five autistic subjects. These subjects, with variable levels of mental retardation, demonstrated marked Purkinje cell loss in the cerebellar hemispheres, together with retained fetal neuronal circuitry in cerebellar nuclei and increased neuronal packing in specific regions of the limbic system, amygdala, and hippocampus. The architecture of the cerebral cortex was not affected. Although our knowledge of brain functioning is incomplete, alterations of the kind noted in the cerebellum and limbic system could reasonably produce autistic behaviors. For more detail, readers are directed to a review of cerebellar contributions to higher functions by Schmahmann (1991). Neuroimaging studies allow less resolution of brain structure than do neuroanatomic studies, and the reported findings from neuroimaging are somewhat contradictory. However, a number of investigators have reported structural abnormalities in ventricle size and cerebral hemispheric asymmetry using CT. MRI, which offers greater resolution, has uncovered some consistent findings, along with a variety of nonspecific abnormalities. Common abnormalities include reduced volume of cerebellar hemispheres and vermal lobules--findings not inconsistent with the above-mentioned neuropathological defects. It is also interesting to note that individuals with fragile X syndrome have similar cerebellar findings. PET and NMR studies of autism are at a preliminary stage, but these methodologies allow insight into the functioning of the brain, rather than simply brain anatomy. Recent PET studies indicating decreased association between paired regions of the brains of autistic subjects are of interest, particularly if they can be confirmed and refined by additional studies. Neurophysiological studies also offer insight into brain function, but are subject to numerous methodological criticisms. Nevertheless, recent reports of diminished P300 waves and absent NC components in autistic subjects seem to indicate fundamental defects in attention and secondary processing, which could help explain the self-stimulatory behaviors often seen in autism. The disturbances in brain development associated with autism can be produced in a number of ways, and at different times during development of the nervous system.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8463065     DOI: 10.1016/s0074-7742(08)60569-3

Source DB:  PubMed          Journal:  Int Rev Neurobiol        ISSN: 0074-7742            Impact factor:   3.230


  16 in total

1.  Prenatal viral infection leads to pyramidal cell atrophy and macrocephaly in adulthood: implications for genesis of autism and schizophrenia.

Authors:  S Hossein Fatemi; Julie Earle; Reena Kanodia; David Kist; Effat S Emamian; Paul H Patterson; Limin Shi; Robert Sidwell
Journal:  Cell Mol Neurobiol       Date:  2002-02       Impact factor: 5.046

2.  Infratentorial brain maturation: a comparison of MRI at 0.5 and 1.5T.

Authors:  K Hittmair; J Kramer; T Rand; G Bernert; D Wimberger
Journal:  Neuroradiology       Date:  1996-05       Impact factor: 2.804

Review 3.  Etiology of infantile autism: a review of recent advances in genetic and neurobiological research.

Authors:  G Trottier; L Srivastava; C D Walker
Journal:  J Psychiatry Neurosci       Date:  1999-03       Impact factor: 6.186

4.  Autistic-like findings associated with a urea cycle disorder in a 4-year-old girl.

Authors:  Işik Görker; Umran Tüzün
Journal:  J Psychiatry Neurosci       Date:  2005-03       Impact factor: 6.186

5.  Behavioral comparisons in autistic individuals from multiplex and singleton families.

Authors:  Michael L Cuccaro; Yujun Shao; Meredyth P Bass; Ruth K Abramson; Sarah A Ravan; Harry H Wright; Chantelle M Wolpert; Shannon L Donnelly; Margaret A Pericak-Vance
Journal:  J Autism Dev Disord       Date:  2003-02

6.  Non-invasive evaluation of the GABAergic/glutamatergic system in autistic patients observed by MEGA-editing proton MR spectroscopy using a clinical 3 tesla instrument.

Authors:  Masafumi Harada; Masako M Taki; Ayumi Nose; Hitoshi Kubo; Kenji Mori; Hiromu Nishitani; Tsuyoshi Matsuda
Journal:  J Autism Dev Disord       Date:  2011-04

Review 7.  Autism: in search of susceptibility genes.

Authors:  Janine A Lamb; Jeremy R Parr; Anthony J Bailey; Anthony P Monaco
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 3.843

8.  Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

Authors:  J Hallmayer; E Pintado; L Lotspeich; D Spiker; W McMahon; P B Petersen; P Nicholas; C Pingree; H C Kraemer; D L Wong
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

9.  Evidence for three subtypes of repetitive behavior in autism that differ in familiality and association with other symptoms.

Authors:  Kristen S L Lam; James W Bodfish; Joseph Piven
Journal:  J Child Psychol Psychiatry       Date:  2008-11       Impact factor: 8.982

10.  Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.

Authors:  Yujun Shao; M L Cuccaro; E R Hauser; K L Raiford; M M Menold; C M Wolpert; S A Ravan; L Elston; K Decena; S L Donnelly; R K Abramson; H H Wright; G R DeLong; J R Gilbert; M A Pericak-Vance
Journal:  Am J Hum Genet       Date:  2003-02-03       Impact factor: 11.025

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