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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 124 (1977), S. 231-256 
    ISSN: 1432-1076
    Keywords: Severe mental retardation ; Etiology ; Family history ; Recurrence risk ; Autosomal recessive
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The family history of 40 patients with severe “pure” mental retardation (MR) was studied to determine the incidence of mental retardation and dull-normal intelligence among relatives, probable etiologies and an empriric recurrence risk. Significant findings include: (1) an increased sex ratio (69% males) of propositi, (2) a significant proportion of patients with clinical manifestations besides MR, (3) virtually no consanguinity among parents, (4) a “positive” family history for over 1/2 of the propositi—about 37% of all children in the sibships were affected; about 21% of the full sibs were affected, (5) a higher number of offspring produced by dull persons and a lower number of offspring from retarded persons compared to two normal persons, (6) a proportionately large number of affected children produced from matings involving one or two dull persons, (7) a tendency for dull persons to have additional dull children and mentally retarded parents to have further retarded children while normal parents with more than one affected child usually had further retarded children, (8) an incidence of affected parents of about 32%, and (9) an overall empiric recurrence risk of 14%. Several etiologies were discussed as possible causes of the condition(s) in this group: (unrecognized) environmental damage and/or maternal/fetal interaction; unrecognized chromosome abnormalities; the homozygous state of several different autosomal recessive genes; X-linked recessive mutations; autosomal dominant new mutations; and multifactorial inheritance. It was concluded that the group was etiologically heterogeneous and although none of the probable etiologies could be excluded, it seemed reasonable to assume that autosomal recessive inheritance plays an important role in the etiology of severe “pure” mental retardation.
    Type of Medium: Electronic Resource
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