Sickle-cell disease primary prevention: Difference between revisions
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{{Sickle-cell disease}} | {{Sickle-cell disease}} | ||
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==Overview== | ==Overview== | ||
There is no specific role for primary prevention in sickle cell disease. | |||
==Primary Prevention== | ==Primary Prevention== | ||
There is no specific role for primary prevention in sickle cell disease because this is a monogenetic disorder. However, genetic counseling for persons who are at high risk for having a child with sickle cell disease can be considered a method of primary prevention. For persons who are heterozygous for the sickle cell allele, education should be provided regarding the probability of having a child with sickle cell disease. A person with sickle cell trait may then chose to make an educated decision about avoiding mating with another person who has sickle cell trait, since there is a 25% likelihood that the offspring will have sickle cell disease (homozygous for the mutation). | |||
==References== | ==References== | ||
Revision as of 19:43, 14 October 2016
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Sickle-cell disease Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Sickle-cell disease primary prevention On the Web |
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American Roentgen Ray Society Images of Sickle-cell disease primary prevention |
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Risk calculators and risk factors for Sickle-cell disease primary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Shyam Patel [2]
Overview
There is no specific role for primary prevention in sickle cell disease.
Primary Prevention
There is no specific role for primary prevention in sickle cell disease because this is a monogenetic disorder. However, genetic counseling for persons who are at high risk for having a child with sickle cell disease can be considered a method of primary prevention. For persons who are heterozygous for the sickle cell allele, education should be provided regarding the probability of having a child with sickle cell disease. A person with sickle cell trait may then chose to make an educated decision about avoiding mating with another person who has sickle cell trait, since there is a 25% likelihood that the offspring will have sickle cell disease (homozygous for the mutation).