Genotype of a woman with hemophilia
WebHemophilia is a recessive sex-linked disease carried on the X chromosome in humans. 3. Write the genotype of a woman who does not have hemophilia. _____ 4. Write the genotype of a woman with hemophilia. _____ 5. Write the genotype of a woman who is a carrier (heterozygous) for hemophilia. _____ 6. Write the genotype of a man who has … A female who inherits one affected X chromosome becomes a “carrier” of hemophilia. She can pass the affected gene on to her children. In addition, a female who is a carrier sometimes can have symptoms of hemophilia. In fact, some doctors describe these women as having mild hemophilia. Females who … See more A woman who is a carrier of the hemophilia gene can have low factor VIII (8) or factor IX (9) levels, and have symptoms of … See more Mothers who carry the hemophilia gene are at risk for serious bleeding after delivery. This is because the high levels of factor VIII during pregnancy fall back to lower levels after … See more
Genotype of a woman with hemophilia
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WebExpert Answer 3.a. Hemophilia is a X-linked recessive disorder which means that the women must carry two defective X allele for the trait to show itself. If H is the defective allele, then the genotype of the woman is X^H X^H. b. Since men … View the full answer Transcribed image text: 3. WebSep 27, 2011 · The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a …
WebHemophilia A (Classic Hemophilia) This type is caused by a lack or decrease of clotting factor VIII. Hemophilia B (Christmas Disease) This type is caused by a lack or decrease of clotting factor IX. Signs and … WebFeb 11, 2024 · since the said that both of them got married and produced a daughter with hemophilia so the only explanation to that is that the mother will be heterozygous dominant for hemophilia which is a carrier for it and also the said that the father has hemophilia also so when the parents mate they will have 50% chance among all of their offspring to be …
WebHemophilia is an X-linked recessive disorder that exists in two forms, hemophilia A and hemophilia B. Hemophilia A is characterized specifically by a mutation on the factor … WebWhat is the genotype of a woman with hemophilia? Hemophilia: Hemophilia belongs to a group of inheritable diseases that involves excessive bleeding and lack of proper coagulation. There are...
WebJan 10, 2024 · What is the genotype of a woman with normal blood clotting whose father had hemophilia? When the offspring do not have a XH and only have the Xh allele/alleles they will have the hemophilia condition. Man’s genotype is XhY. Daughter’s genotype is XHXh (She got the Xh from her father. She has a normal phenotype, so we know her …
WebAlthough females with severe or moderate HB are quite rare, women and girls made up 24% of individuals with mild HB seen for care at US HTCs. 44 The genetic causes of … pineberry shoppeWebA woman who is heterozygous for hemophilia marries a normal male. What are the possible phenotypes of their children? Show the Punnett Square! g. A woman who is a carrier for hemophilia marries a man with hemophilia. Could any of their children have hemophilia? If so, would the child be male or female? Show the Punnett Square (s)! pineberry789WebThe hemophilia gene can occur in a man or woman this way. The blood clotting gene suddenly becomes faulty. The gene may be passed by female carriers for several generations before hemophilia appears in a boy … top places to visit vancouverWebHemophilia is most commonly propagated within a line when asymptomatic carrier females are bred to normal males. The male puppies produced from this mating with each have a … pineberry shoppe brown city miWebA phenotypically non-bald woman and a bald man produce four bald sons and a non-bald daughter. What are the most likely genotypes of the mother and father? bb and bb bb … top places to work in charlotte ncWebFeb 26, 2024 · Explanation: A female with hemophilia would have to have her 2 sex chromosomes (the two X's), or pair 23, with the hemophilia alleles. Those alleles cannot … pineberry solarWebApr 9, 2024 · Haemophilia was previously regarded as a classical example of Mendelian inheritance, with mutation in only a single gene (F8 or F9) causing the disease phenotype. The disease manifests complete penetrance. Studies, however, revealed the striking genetic and phenotypic heterogeneities of the disease. pineberry strain