Explain the following 1. A couple comes to a genetic councilor concerned about their chances of having a baby with cystic fibrosis disease. The husband had a sibling die of the disease. What are the chances that he is a carrier?

Q: 14. Write the karyotype of a Turner syndrome. O A) 2n = 46 - 1 O B) 2n - 1 = 45 O C) 45, X O D) 46 -…

A: Karyotype is defined as the combination of the chromosomes of an individual. It is a laboratory…

Q: What is the genotype of individual 12? O AA or Aa O AA O Aa aa

A: Autosomal genes are present on the chromosome. The dominant gene will express itself in presence of…

Q: Marfan syndrome is inherited in an autosomaldominant pattern. Which of the following is true?a.…

A: Marfan syndrome refers to a genetic disorder of the connective tissue. The extent to which the…

Q: use the following information: type A hemophilia, a disorder in which blood does not clot properly,…

A: Hemophilia is a rare disorder in which the blood doesn't clot normally because it lacks sufficient…

Q: 1. Below given is a pedigree for hemophilia. Find the genotype and the phenotypes of the parents.

A: Inheritance is the phenomenon of passing on the traits from parents to their offspring. Traits are…

Q: i) A couple each having sickle cell trait have five children. What is the probability that they will…

A: Sickle cell disease (SCD) is a genetic disorder that follows the autosomal recessive pattern of…

Q: What is Patient A's karyotype? A. Down syndrome B. Patau syndrome C. Klinefelter syndrome D.…

A:

Q: Which genotype indicates an individual II/2? O xCx O xCy O XX OXY

A: Traits which are determined by alleles present on the X chromosomes are referred to as X- linked…

Q: A couple comes to a genetic councilor concerned about their chances of having a baby with cystic…

A: Cystic fibrosis is a progressive, genetic disease that impairs the lungs and digestive system. It is…

Q: Imagine you are working as a genetic counselor. A married couple makes an appointment to speak with…

A: BASIC INFORMATION  MODES OF INHERITENCE 1. AUTOSOMAL DOMINANT INHERITENCE In this each generation is…

Q: Describe both the primary gene or protein defect and the resulting phenotype for the following…

A: A)Cystic fibrosis is an autosomal recessive disease.It is a progressive disease and requires daily…

Q: Case 2: Polycystic Kidney Disease (dominant lethal allele) Maria is 38 years old. She and her…

A: Given the following information in the question -  The disease is autosomal dominant  Maria's…

Q: Rewrite the following sentences after correction. (03 marks) If one parent has sickle cell anemia…

A: Sickle cell anemia: It is basically a red blood cells disorder because there is occurrence of moon…

Q: 3. Charles and Camilla are planning to start a family. Camilla has Huntington's disease. Charles…

A: Introduction :  Huntington's disease is an autosomal dominant pattern, which means one copy of the…

Q: Kathy's brother has cystic fibrosis. Her husband has no family history of CF. What is the chance…

A: The genetic condition cystic fibrosis (CF) affects the lungs, digestive system, and other body…

Q: When we say that a woman is a carrier for a genetic disease or disorder it means that     a. she can…

A: Genetic disorders follow a particular pattern of inheritance. They can follow autosomal recessive,…

Q: B- Find the determinate 1 B – 2 e - 7 3. 3

A: we are answering only part B  Pls repost for part A with clear image.

Q: 2. Describe the phenotype of individuals whe inherit two copies of the Hbs allele whq Sickle-Cell…

A: * sickle cell Anemia a is blood disorder due to mutation will leads to change in shape of cells into…

Q: Mary and Ron don’t have albinism. However, is it possible for them to have a child with albinism?…

A: Albenism Albinism refers to the decolourise of the skin hair and eye. it is a very rare recessive…

Q: Normal growth and development in children can be changes with the disease. Eplain the influences…

A: Cystic fibrosis chronic hereditary disease. This condition may casuse the thickening of the mucus,…

Q: Two parents with sickle-cell trait have a child. What is the chance that the child has sickle-cell…

A: Humans contain twenty two pairs of autosomal chromosomes and one pair of sex chromosomes. A female…

Q: If a person is heterozygous for cystic fibrosis is married to someone who actually has the disease.…

A: Cystic fibrosis is an autosomal recessive genetic disease.   So,the person homozygous for cystic…

Q: A man with hemophilia has a daughter of normal phenotype. She marries a man who is normal for the…

A:

Q: Why is the chances of having a child with down's syndrome increases if the age of mother exceed…

A: Down’s syndrome is basically an autosomal genetic disorder that is caused by trisomy at chromosome…

Q: An affected daughter An unaffected daughter Ginger is pregnant with a fifth child, a son.  What is…

A: The Lalaphobia is the disease just like Colourblindness  means it is an sex linked recessive disease…

Q: Cleft lip and cleft palate can be a devastating congenital disorder. Please explain why this…

A: A congenital disorder is an inherited medical disorder that occurs in a baby at or before birth.…

Q: 10. If the woman is type O and the father is type AB. % AB % A % B % O

A: Mother Father   A B O OA OB O OA OB

Q: Answer the following questions. 1. Why are males more likely than females to have sex-linked…

A: Since there are multiple questions in this particular question, I'll answer the first three subtypes…

Q: One difference between Huntington's disease and the other three neurodegenerative disorders…

A: Huntington disease like Parkinson's disease Alzheimer's disease and Lu gehrigs disease are all neuro…

Q: 12 1 I1 2 I1:3 I1:4 I1.5 I1 6 I:7 III 2 III:3 II 4 III:5 III.6

A: Many people refer to problems with one’s ability to see color as color blindness, however, unless a…

Q: A 16-year-old girl appealed to the genetic consultation. She complains about menstruation absence.…

A: Introduction There are various genetic disorders that develop due to anomalies in sex chromosomes.…

Q: While studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this…

A: Introduction :- Hypertrichosis, which can affect both men and women, is described as excessive hair…

Q: Stephanie has normal color vision. Her husband Chris also has normal color vision. They have a son…

A: Color blindness is the diminished capacity to see tone or contrasts in shading. It can weaken such…

Q: 3) State whether each of the following genetic defects is inherited as an autosomal recessive,…

A: Introduction :- DNA acts as the genetic material of the cell , that stores all the hereditary…

Q: A woman who is a carrier for cystic fibrosis (CF), an autosomal recessive disorder, has children…

A: Cystic fibrosis is a genetic disorder which is caused by the mutation in the CFTR gene which codes…

Q: What is the relationship between individual I-1 and individual III-2? Incidence of Hemophilia…

A: Introduction Haemophilia Is A Hereditary Condition That Affects The Body's Capacity To Form Blood…

Q: The mode of inheritence for this disease is recessive 1 II 4. III 3 4 6. 8 9. 10 IV 13 O Yes O No

A: Pedigree is a family tree drawn with standard genetic symbols (like genetical table, chart or…

Q: 1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the…

A: Hemophilia  A X linked recessive disorder. The person suffering from hemophilia lack blood clotting…

Q: What is Apert syndrome? Are there variations of this genetic disorder? What are the symptoms and…

A: “Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: What is the chance for each child to have Huntington's disease? Are the 3 events (the children…

A: a. What is the chance for each child to have Hungtington's disease? As the disease is dominant each…

Q: (1) What is the karyotype for men who have an extra Y chromosome? Discuss all the ways you can test…

A: INTRODUCTION A chromosomal disorder results in a change in the number of chromosomes in the body.…

Q: What is Patient C's karyotype? A. Last song syndrome B. Trisomy 21 C. Marfan syndrome D. Patau…

A: A karyotype is a collection of a species' or an individual organism's full set of metaphase…

Q: What are the chances that Ann and Michael next child will have the disease. Assume people marrying…

A: Pedigree analysis The formal study of the pattern of a trait in a pedigree to determine such…

Q: What is Patient B's karyotype? A. Klinefelter syndrome B. Trisomy 13 syndrome C. Down syndrome…

A: Introduction : Karyotype : Karyotype is a representation of  complete set of metaphasic chromosome…

Q: 9) A husband and wife are both carriers for cystic fibrosis. What are the chances their son will…

A: Cystic Fibrosis ---Cystic Fibrosis is a genetic disease caused by abnormal gene ,which occurs due to…

Q: 4. (a) Give the possible blood groups of the following crosses? a. O x A b.A x AB c. Ax B d.B x B e.…

A: Question - 4(a) - Give the possible blood groups of the following crosses? a. Ox A b.AX AB c. AXB d.…

Q: Please answer with reason: 5) The nurse explains to parents that if both of them are…

A: Autosomal Recessive disorder:              In-order to possess autosomal recessive disorder,…

Q: what is the probability that he would be affected with dark blue skin colo

A: The Ankura race of Gunguns on the planet Naboo are affected with an inherited genetic disorder…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.