Infantile autism, as defined by the international criteria presently adopted in accordance with the DSM III-R, comprises forms that differ not only in etiology, as generally accepted, but also from the behavioural viewpoint. This paper presents a group of 15 patients, aged 2 - 8 years, assessed by plotting findings on a chart from which the true 'autistic' component (a specific defect in interpersonal relations) could be determined and isolated from possible defective components. The following activities were assessed by analyzing a series of videotape recordings: play, mimic gestural expressivity, smiling, eye contact, language, interpersonal relations. Three groups of cases were described: (1) Rett's syndrome (as a typical example of the autistic condition in progressive neurologic illness); (2) defective low-functioning conditions ('autism' associated with non-evolutive brain damage and/or mental retardation); (3) primary high-functioning conditions, or Kanner's autism (without any evidence of organic brain damage and with normal or only slightly retarded mental development). The factors recognizable as true 'autism' are always present and predominant in group 3, inconsistent in group 2 and absent in group 1.
BEHAVIORAL-PATTERNS IN INFANTILE-AUTISM - A CONTRIBUTION TO THE DEBATE ON A UNITARY SYNDROME
DE NEGRI, MAURIZIO;BAGLIETTO, MARIA GIUSEPPINA
1994-01-01
Abstract
Infantile autism, as defined by the international criteria presently adopted in accordance with the DSM III-R, comprises forms that differ not only in etiology, as generally accepted, but also from the behavioural viewpoint. This paper presents a group of 15 patients, aged 2 - 8 years, assessed by plotting findings on a chart from which the true 'autistic' component (a specific defect in interpersonal relations) could be determined and isolated from possible defective components. The following activities were assessed by analyzing a series of videotape recordings: play, mimic gestural expressivity, smiling, eye contact, language, interpersonal relations. Three groups of cases were described: (1) Rett's syndrome (as a typical example of the autistic condition in progressive neurologic illness); (2) defective low-functioning conditions ('autism' associated with non-evolutive brain damage and/or mental retardation); (3) primary high-functioning conditions, or Kanner's autism (without any evidence of organic brain damage and with normal or only slightly retarded mental development). The factors recognizable as true 'autism' are always present and predominant in group 3, inconsistent in group 2 and absent in group 1.
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