Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
West J Med ; 124(1): 6-12, 1976 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-946335

RESUMO

The geographic distribution of County Health Department clinic facilities in the state of California has made it readily possible to establish a regionalized program for genetic counseling services, using public health nurses as a major source of case-finding. From both consumer and health professional standpoints, regionalized satellite genetic counseling clinics have been successful, and in particular, the effectiveness of public health nurses in identifying clinical genetic problems is readily apparent.Long-term follow-up reinforcement of genetic counseling appears to be an important conclusion from these studies. It is our suggestion that reinforcement of counseling would best be accomplished through the health team member (physician, nurse and so forth) following the patient or family rather than through the consulting geneticist.


Assuntos
Aconselhamento Genético , Ambulatório Hospitalar/normas , United States Public Health Service , Adulto , California , Aberrações Cromossômicas/prevenção & controle , Transtornos Cromossômicos , Estudos de Avaliação como Assunto , Humanos , Risco , Estados Unidos
2.
West J Med ; 123(1): 17-21, 1975 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-1154778

RESUMO

This report describes the first antenatal diagnosis of an XXX female. Over 150 postnatal cases of XXX females have been described. There is no specific phenotype associated with the sex chromosome abnormality and most such persons are fertile. The frequency of XXX females in mental institutions is 3.9 per 1,000 female subjects whereas the frequency in consecutive newborn infants is 1.1 per 1,000 newborns. Chi-square analysis shows this difference cannot be due to chance. On the other hand, data from consecutive newborn studies suggest that intellectual development in XXX newborns is within normal range. Available evidence favors normal development in XXX female infants although the risk for developmental disabilities may be higher for the XXX than for the XX infant.


Assuntos
Aconselhamento Genético , Diagnóstico Pré-Natal , Aberrações dos Cromossomos Sexuais/diagnóstico , Adolescente , Feminino , Humanos , Recém-Nascido , Cariotipagem , Gravidez
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...