Explain the pattern of hemophilia in …
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Meghna Thapar 5 years, 2 months ago
Hemophilia is a rare blood disease that usually occurs in males. In fact, it's extremely rare for women to be born with the condition because of the way it's passed down genetically. A female would need to inherit two copies of the faulty gene — one from each parent — to develop hemophilia A, B or C. Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes associated with these conditions are located on the X chromosome, which is one of the two *** chromosomes. ... In X-linked recessive inheritance, a female with one altered copy of the gene in each cell is called a carrier.
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