WebHemophilia A (HA, MIM no. 306700) is an inherited, recessive, X-linked bleeding disorder caused by a wide spectrum of mutations in the gene encoding coagulation factor VIII ( F8 gene). HA affects 1 in 5000 males. The F8 gene has a span of approximately 186 kb on chromosome X at locus q28 and consists of 26 exons [ 1 ]. WebHemophilia A, also called factor VIII (8) deficiency or classic hemophilia, is a genetic disorder caused by missing or defective factor VIII (FVIII), a clotting protein. Although it …
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WebHemophilia is a blood disorder caused by an X-linked recessive trait. A man with hemophilia and a woman who does not have hemophilia and is not a carrier for the trait … WebHemophilia A is caused by having low levels of a protein called factor VIII. Factor VIII is needed to form blood clots. The disorder is inherited in an X-linked recessive manner … see iphone autofill credit cards
Solved 6. Hemophilia is a sex-linked trait. A person with - Chegg
WebQuestion 4 (1 point) Hemophilia is a blood-clotting disorder, and one type of hemophilia is caused by a recessive X-linked allele. A man and woman with normal blood-clotting … WebHaemophilia exists in two forms: Hemophilia A: It is caused specifically by a mutation in the Factor VIII gene on the X chromosome. Hemophilia B: This is caused by a mutation … WebSo, the cause of the abnormality is non-disjunction in anaphase I or II. The karyotype shows unequal X and Y chromosomes ( Choice A and B ), but this is normal for a human karyotype. The sex chromosomes are not homologous. Crossing over in prophase I ( Choice B and Choice D) exchanges genetic material between two nonidentical sister chromatids. put enmity between thy seed