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Dictionary » R » Rh disease Rh diseaseDefinition noun A type of hemolytic disease of the fetus or newborn which involves the incompatibility of the Rhesus blood group of the mother and her offspring.
For example, the mother is rH- while the fetus is rH+. It results in the immune system of the rH- mother to produce antibodies that enter fetal circulation and attack the red blood cells of the rH+ fetus, resulting in the hemolysis and anemia in fetus. Symptoms include jaundice, anemia, enlarged liver and spleen.
See also: erythroblastosis fetalis, Rhesus blood group ![]()
Please contribute to this project, if you have more information about this term feel free to edit this page ![]()
Results from our forummutation-selection balance... equation. Here are two relevant excerpts from my textbook, Medical Gentics by Jorde, Carey and Bamshad: Consider, for example, a dominant disease that results in death before the person can reproduce. This is termed a genetic lethal mutation because, even though the individual might survive ...
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Re: mutations and dependencies... part of the whole thing (BILLIONS of functionally sequenced nucletoide base pairs that given a single letter change may kill someone/give them a disease). 2 weeks of solid reading is all it would take if someone wanted to know the TRUTH about origins though the implications may not agree with ...
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Re: mutations and dependencies... part of the whole thing (BILLIONS of functionally sequenced nucletoide base pairs that given a single letter change may kill someone/give them a disease). 2 weeks of solid reading is all it would take if someone wanted to know the TRUTH about origins though the implications may not agree with ...
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Help??? Genetics problem cannot figure it out?... defective and one X normal (from mother). In 30% of cell divisions the chromosomes recombine and form two defective X chromosomes (each for other disease, but they ask for normal kid, so any of these chromosomes will be ruled out). In the other 70% cases the chromosome will be defective in 50% ...
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Re: Muscular dystrophy inheritance questionThis might get you partway there. Dystrophin is a sex-linked disease carried on the X (sex) chromosome. It behaves as a recessive in females (who have two alleles for dystrophin) and as a dominant in males (who have only one dystrophin gene on their single ...
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