Autosomal Dominant is a mutation in one copy of the gene. It is inherited from an affected parent or arises de novo. Group of answer choices Both statements are incorrect Statement 1 is correct. Statement 2 is incorrect Statement 2 is incorrect. Statement 1 is correct Both statements are correct

Autosomal Dominant is a mutation in one copy of the gene. It is inherited from an affected parent or arises de novo. Group of answer choices Both statements are incorrect Statement 1 is correct. Statement 2 is incorrect Statement 2 is incorrect. Statement 1 is correct Both statements are correct

Name: Autosomal Dominant is a mutation in one copy of the gene. It is inheri
Uploaded: 2024-03-20T06:43:04.000Z
Channel: Bartleby
Description: Autosomal Dominant is a mutation in one copy of the gene. It is inherited from an affected parent or arises de novo. Group of answer choicesBoth statements are incorrectStatement 1 is correct. Statement 2 is incorrectStatement 2 is incorrect. Stateme

Medical Terminology for Health Professions, Spiral bound Version (MindTap Course List)

8th Edition

ISBN:9781305634350

Author:Ann Ehrlich, Carol L. Schroeder, Laura Ehrlich, Katrina A. Schroeder

Publisher:Ann Ehrlich, Carol L. Schroeder, Laura Ehrlich, Katrina A. Schroeder

Chapter2: The Human Body In Health And Disease

Section: Chapter Questions

Problem 17LE

See similar textbooks

Similar questions

A couple has had a child born with neurofibromatosis. They come to your genetic counseling office for help. After taking an extensive family history, you determine that there is no history of this disease on either side of the family. The couple wants to have another child and wants to be advised about the risks of that child having neurofibromatosis. What advice do you give them?
Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of an individual with achondroplasia is seeking counsel on the likelihood of his being a carrier of the mutant allele. What is the probability that the unaffected client is carrying the achondroplasia allele?
In autosomal dominant, A child who has a parent with the mutated gene has a 50% chance of inheriting that mutated gene. Likewise, there is a 50% chance of having an unaffected child Group of answer choices Both statements are correct Statement 1 is incorrect, statement 2 is correct Statement 1 is correct. Statement 2 is incorrect Both statements are incorrect
You met with two parents whose first child has sickle cell anemia. (The parents show no signs of the disease themselves). The mother comes to you in the third month of her second pregnancy, and wants to know if this child will also inherit the disease. As a genetics counselor, you are ready to evaluate this couple’s case by doing the following:1. Determine what the genotype of each parent is. Is this disease autosomal or sex-linked? Dominant or recessive?
One of your patients, a six-year-old girl who suffers from Sickle cell anemia, an inherited blood disorder in which red blood cells are abnormally shaped and fragile, leading to a short supply of red blood cells. These abnormal cells can also get stuck in small vessels, which prevent blood flow, leading to fatigue, pain and other severe complications. Sickle cell anemia is an autosomal recessive disorder. Neither of your patient's parents has sickle cell anemia. What is the most likely genotype of her parents? (The normal beta-globin allele is abbreviated as B, and the abnormal allele as b.) one is B and one is b one is BB and one is bb both are Bb both are bb both are BB
Imagine you are working as a genetic counselor. A married couple makes an appointment to speak with you. Both have a genetic disorder, but they already have one child who does not have the disorder. They would like to have more children and were told by a friend that since their first child was normal their future children would be normal as well.Explain to them the probability of future offspring being normal or having the disease (assume that this is an autosomal disease). Be sure to tell them whether the disease is brought about by a dominant or recessive allele and what fraction of their children (if any) could be carriers for the disease.I
Imagine you are working as a genetic counselor. A married couple makes an appointment to speak with you. Both have a genetic disorder, but they already have one child who does not have the disorder. They would like to have more children and were told by a friend that since their first child was normal their future children would be normal as well. Explain to them the probability of future offspring being normal or having the disease (assume that this is an autosomal disease). Be sure to tell them whether the disease is brought about by a dominant or recessive allele and what fraction of their children (if any) could be carriers for the disease.
Joe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for this disease from the following people? Yes No a. His mother’s mother ____________ ____________ b. His mother’s father ____________ ____________ c. His father’s mother ____________ ____________ d. His father’s father ____________ ____________
Color-blindness is an X-linked recessive disorder. Under what circumstances will this condition manifest in a child? Top of Form If the child is a male and its mother has the recessive allele If the child is a female and its father has the recessive allele If the child is a female and its mother has the recessive allele If the child is a male and its father has the recessive allele
Duchenne muscular dystrophy is one of the sex-inherited disease. Write a report about the mutation that caused the disease, symptoms, genetics therapies, include a minimum of one human pedigree that show the disease
Soft toenail is an extremely rare recessive disorder. Mike whose aunt (his mother's sister) has the condition marries Phoebe whose niece (her brother's daughter) is affected by the condition. No one else in either family has the condition. asap
When an individual has genome mutations, their chromosome structure changes. True or False.