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Familial tendencies in diseases of children

Datos Bibliográficos

ID11181663
AutoresHoward B Newcombe (autor de correspondencia)
Año1966
Volumen20
Número2
Páginas49-57
Fecha de publicación1966-04-01
Open AccessNo
TipoARTICLE
RevistaJournal of Epidemiology and Community Health (JOURNAL)
Identificadores de la revistaISSN: 0143-005X • E-ISSN: 1470-2738
EditorialBMJ (PUBLISHER • GB)
DOI10.1136/jech.20.2.49
PMID6006379
OpenAlexW1984621680
IdiomaEN
Citas recibidas5
Referencias citadas3

The clustering of cases of disease within family groups has long been of interest to geneticists, but the empirical data which they have gathered con cerning the strengths of these associations have had to do largely with conditions that were thought in advance to be either hereditary or at least partially so. Epidemiologists, who might be expected to be interested in the strengths of familial predispositions other than those due to heredity, have perhaps lacked the specific motivation of the geneticists and have certainly been hampered as well by a lack of appropriate methods for quantitative study of the problem on any substantial scale. Conventional sampling techniques, for example, tend to be unsuitable for studies of recurrences of similar events of ill health among different members of the same families, and are especially so where the diseases in question are rare. Although this particular obstacle to investigation of the familial component of ill health might be avoided by the use of routine records of illnesses and of family compositions covering whole populations, such records have not in the past been organized in a manner that would facilitate quantitative studies of the special risks to relatives of affected individuals. Methods are now available, however, for obtain ing family histories of procreation and of mortality and morbidity from the routine records of vital and health events, throughout whole registration areas (Kennedy, 1961, 1962; Kennedy, Newcombe, Okazaki, and Smith, 1965; Newcombe and Kennedy, 1962; Newcombe, Kennedy, Axford, and James, 1959). Such methods have been used in the present study to measure the strengths of the family asso ciations of a wide range of ailments, including many that are caused mainly by environmental factors or for which there is currently little evidence of an hereditary component in the aetiology

Disease · Family medicine · Heredity · Pathology · Child and Adolescent Health · Global Public Health Policies and Epidemiology · Medicine · Nutrition, Genetics, and Disease

  • Reproductive Patterns after Stillbirth and Early Infant Death

    Open Access•H P Vogel, E G Knox•Journal of Biosocial Science•1975

  • Twinning and anencephaly

    Open Access•William H James•Annals of Human Biology•1976

  • The combined use of a central registry and vital records for incidence studies of congenital defects

    D H Renwick, D H G Renwick•Journal of Epidemiology and…•1968

  • Epidemiology and family characteristics of severely-abused children

    J A Baldwin, J E Oliver et al.•Journal of Epidemiology and…•1975

  • The prevention of genetic disease in the population

    Alan E H Emery•International Journal of…•1972

  • Social Implications of the 1947 Scottish Mental Survey

    Adam Curle, John Nisbet et al.•British Journal of Educational…•1954

  • Social Implications of the 1947 Scottish Mental Survey

    Ruth Riemer, James Maxwell•American Sociological Review•1954

Citas por año0,09
Intervalo de citas1968 - 1976 (9)
Altamente citadoNo

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