18. Regressive autism

    1 - Heller and Landau-Kleffner disorders
    2 - Rett and :Leigh syndromes
    3 - Schizophrenia spectrum disorders
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Heller (1908) and DeSanctis (1908) described "dementia infantilis" more than three
decades earlier than Kanner (1943).  The designation dementia infantilis was made in
the context of Kraepelin's dementia praecox (Kraepelin (1904), implying emergence of
psychotic behavior early in childhood.  Dementia praecox (later superseded by the
euphemism schizophrenia) usually first appears in adolescence or early adulthood.  
Landau and Kleffner (1957) described an autistic-like condition associated with onset
of seizure disorder, in which previously acquired language is lost.  The core syndrome
of Kanner autism differs from the syndromes of Heller, DeSanctis, and
Landau-Kleffner in that social isolation exists from birth and seizures are not a part of
Kanner autism.
Contents
Views of
Autism
Language
Disorder
Neurologic
Impairments
Research
Chronology
References
Notes
Index
Links
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Introduction
Home
Blog
Preface

III -
EVIDENCE OF NEURO-
LOGICAL  IMPAIRMENTS
9.   The nature of autism
10. Language and hearing
11. The auditory system
12. Brainstem nuclei
13. Perinatal vulnerability
14. Brainstem damage
15. Neuropathology
16. Fetal alcohol syndrome
17. Phenylketonuria
18. Regressive autism

<<
Heller & Landau-Kleffner
disorders
Rett and Leigh
syndromes
Schizophrenia
spectrum disorders