Hemophilia is a genetic condition that results in lthe lack of a clotting factor, usually facto...
Hemophilia is a genetic condition that results in lthe lack of a clotting factor, usually facto viii. What impact would this have on the homeostasis of an individual? Would it matter which factor is missing?
Homework Answers
Haemophilia : in haemophilia cases defect of the in which prevent blood clotting.bacause of prevent blood clott during small cut person bleed and death from the minor skin cut.
This genetic disorder caused by recessive genes in which homeostasis balance not maintain properly because of process of homeostasis all body internally balance that include osmoregulation (Water balance) and other necessary fluid .
Haemophila impact by homeostasis:
1)individual not able to maintain fluid iside the body.
2)Not proper maintenance of water.
3)No proper PH level
4)abnormal functioning during transportation Heat,Water,nutrient and also Nitrogenous waste .
If factor is missing individual not able to achive above mentioned points.
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Hemophilia is a genetic condition that results in lthe lack of a
clotting factor, usually facto...
Hemophilia is a genetic condition that results in the lack of a clotting factor, usually facto...
Hemophilia is a genetic condition that results in the lack of a clotting factor, usually facto viii. What impact would this have on the homeostasis of an individual? Would it matter which factor is missing?
Hemophilia A is a genetic disorder of recessive X chromosome mutation of the Factor VIII gene...
Hemophilia A is a genetic disorder of recessive X chromosome mutation of the Factor VIII gene that causes a blood clotting protein Factor VIII missing or deficient. If a person with XY chromosomes is affected by Hemophilia A and a person with XX chromosomes is an unaffected person, what is the probability that their male offspring might be hemophilic and what is the probability that their female offspring might be carriers of the mutated gene?
Hemophilia is an X linked recessive condition in humans (Xh). Blood type (AB) is determined utilizing...
Hemophilia is an X linked recessive condition in humans (Xh). Blood type (AB) is determined utilizing multiple alleles of I, two of which are codominant. A widow's peak is determined by a single dominant allele (W), while the recessive phenotype is a straight hairline. The ability to taste PTC is determined by a single dominant allele (T). while the recessive phenotype is a non-taster. Eugene is a non-taster male who does not have hemophilia. He has AB blood and a...
Paragraph Styles The technological approaches applied for ancient DNA study can also be used for forensic...
Paragraph Styles The technological approaches applied for ancient DNA study can also be used for forensic genetic analysis in difficult cases where only microscopic amounts of material are available or the DNA has been severely damaged. Some of these approaches were used in the genetic expertise of the putative remains of the family of the last Russian Emperor Nicholas II Romanov. There is historical evidence that Prince Alexey suffered from severe bleeding that is characteristic of hemophilia. It is now...
3. (35 pts) The gene for the cone photoreceptor in the eye and the gene for...
3. (35 pts) The gene for the cone photoreceptor in the eye and the gene for a blood-clotting factor are both in the X-chromosome. Suppose they are 14 map units apart. Mutation in the photoreceptor gene results in color blindness, and is inherited as an X-linked recessive trait. Mutation in the clotting factor gene results in hemophilia, and is also inherited as an X-linked recessive trait. You have two patients: Sally and Jill. Both patients have a family history of...
Question 5 1 pts There is a genetic condition in which the enzyme at #1 is...
Question 5 1 pts There is a genetic condition in which the enzyme at #1 is non-functional. What would be the result of this condition? a. The person would not be able to store glucose as glycogen b. The person would not be able to store glucose as fat c. The person would have a difficult time increasing blood sugar between meals d. The person would be suffering from diabetes e. The person would not be able to eat excess...
question 5-52 93 Dd D) dd D) aa x aa C) human height E) DI 4.Which...
question 5-52
93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...
Name Sex-linked traits are genetic char segments of DNA found on chromosomes that Sex-Linked Traits Senetic...
Name Sex-linked traits are genetic char segments of DNA found on chromosomes that Sex-Linked Traits Senetic characteristics determined by genes located on sex chromosomes. Genies are and on chromosomes that carry information for protein production and that are sponsible for the inheritance of specific traits Genes exist in alternative forms called alleics. or a trail is inherited from each parent Like traits originating from genes on autosomes (non-se chromosomes), sex-linked to omosomes), sex-linked traits are passed from parents to offspring...
FILL-IN-THE-BLANK 4. An extra copy of chromosome 21 results in the genetic condition known as Directions: Supply th...
FILL-IN-THE-BLANK 4. An extra copy of chromosome 21 results in the genetic condition known as Directions: Supply the information requested A problem with the outer or middle ear typically is associated with afn) 1. A guide dog, signal dog or other animal 5. ndividualy trained to provide assistance to an individual with a disability is called afn) hearing loss animal A person becomes overwhelmed and starts throwing things and striking out. The person is exhibiting af) 6. 2. The sensations...
I need answers for 5 to 8. thank you 5. It is probable that a probability...
I need answers for 5 to 8. thank you
5. It is probable that a probability question is in the future From the cross AaBbceDdEell X AABECcDdeer what is the probability of obtaining the genotype AabbCcDDEeff in the progeny? 6. Fill in XY female Cri du Chat Down syndrome XX male Anhydrotic ectodermal dysplasia Patau syndrome Hemophilia Polydactyly Phenylketonuria Achondroplasia Alkaptonuria a) Develop male structure, but experiences infertility b) Develop female structures but may not have ovaries c) Female heterozygotes...
Hemophilia is an X linked recessive condition in humans (Xh). Blood type (AB) is determined utilizing multiple alleles of I, two of which are codominant. A widow's peak is determined by a single dominant allele (W), while the recessive phenotype is a straight hairline. The ability to taste PTC is determined by a single dominant allele (T). while the recessive phenotype is a non-taster. Eugene is a non-taster male who does not have hemophilia. He has AB blood and a...
Paragraph Styles The technological approaches applied for ancient DNA study can also be used for forensic genetic analysis in difficult cases where only microscopic amounts of material are available or the DNA has been severely damaged. Some of these approaches were used in the genetic expertise of the putative remains of the family of the last Russian Emperor Nicholas II Romanov. There is historical evidence that Prince Alexey suffered from severe bleeding that is characteristic of hemophilia. It is now...
Question 5 1 pts There is a genetic condition in which the enzyme at #1 is non-functional. What would be the result of this condition? a. The person would not be able to store glucose as glycogen b. The person would not be able to store glucose as fat c. The person would have a difficult time increasing blood sugar between meals d. The person would be suffering from diabetes e. The person would not be able to eat excess...
question 5-52
93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...
Name Sex-linked traits are genetic char segments of DNA found on chromosomes that Sex-Linked Traits Senetic characteristics determined by genes located on sex chromosomes. Genies are and on chromosomes that carry information for protein production and that are sponsible for the inheritance of specific traits Genes exist in alternative forms called alleics. or a trail is inherited from each parent Like traits originating from genes on autosomes (non-se chromosomes), sex-linked to omosomes), sex-linked traits are passed from parents to offspring...
FILL-IN-THE-BLANK 4. An extra copy of chromosome 21 results in the genetic condition known as Directions: Supply the information requested A problem with the outer or middle ear typically is associated with afn) 1. A guide dog, signal dog or other animal 5. ndividualy trained to provide assistance to an individual with a disability is called afn) hearing loss animal A person becomes overwhelmed and starts throwing things and striking out. The person is exhibiting af) 6. 2. The sensations...
I need answers for 5 to 8. thank you
5. It is probable that a probability question is in the future From the cross AaBbceDdEell X AABECcDdeer what is the probability of obtaining the genotype AabbCcDDEeff in the progeny? 6. Fill in XY female Cri du Chat Down syndrome XX male Anhydrotic ectodermal dysplasia Patau syndrome Hemophilia Polydactyly Phenylketonuria Achondroplasia Alkaptonuria a) Develop male structure, but experiences infertility b) Develop female structures but may not have ovaries c) Female heterozygotes...
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