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dc.contributor.author Tuvman, Estelle en
dc.date.accessioned 2013-10-30T21:50:06Z en
dc.date.available 2013-10-30T21:50:06Z en
dc.date.copyright 1972 en
dc.date.issued 1972-06 en
dc.identifier.uri http://hdl.handle.net/10211.2/4340 en
dc.description Includes bibliographical references (pages 73-77) en
dc.description.abstract Sickle cell anemia is one of the most common long term illnesses of black children. It is an incurable illness which is serious at any age but often fatal during childhood. Approximately one black person in twelve carries the sickle cell trait and the sickle cell anemia is thought to occur in one in five hundred births (44). Sickle cell anemia has been called the "neglected disease”. Until this year, there have been limited efforts to screen and educate the black community about the nature of the genetic disease. Since the disease is as yet incurable, prevention is the only present medical alternative. This thesis was concerned with the measurement of present knowledge of the sickle cell disease in a black community with the expectation that the findings would be of value in future program planning. The hypothesis of the study asked if people who came in for sickle cell screening tests, at a local Health Center, were significantly more knowledgeable about the disease than other groups of persons who used the services of the same Health Center , A questionnaire was administered to a total population of one hundred persons . Both of the sample groups were black and of a low socio-economic background, the results of the statistical analysis revealed that no significant differences in knowledge existed between the two groups. The hypothesis was therefore rejected. Findings of the study showed that the groups studied did not know the difference between the sickle cell trait and the sickle cell anemia; they were unfamiliar with the symptoms of sickle cell anemia, and they believe that people with sickle cell anemia do not live long. It was recommended on that basis of the study that massive educational programs be implemented in the community and the schools in conjunction with sickle cell screening programs and genetic counseling . en
dc.description.statementofresponsibility by Estelle Tuvman en
dc.format.extent viii, 90 pages en
dc.language.iso en_US en
dc.publisher California State University, Northridge en
dc.rights.uri http://scholarworks.csun.edu/xmlui/handle/10211.2/286 en
dc.subject Sickle cell anemia--United States--History--20th century. en
dc.subject.other Dissertations, Academic -- CSUN -- Health Science en
dc.title Knowledge levels of sickle cell anemia within the black community en
dc.type Thesis en
dc.contributor.department California State University, Northridge. Department of Health Science en
dc.description.degree M.P.H. en


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